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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
mRNA and Protein(s)
-
NM_001078650.3 → NP_001072118.1 transmembrane protein 134 isoform b
See identical proteins and their annotated locations for NP_001072118.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) lacks an alternate in-frame exon in the 3' coding region, compared to variant 1. This results in a shorter protein (isoform b), compared to isoform a.
- Source sequence(s)
-
AA830850, AP003419, BC125134, HY053672
- Consensus CDS
-
CCDS41678.1
- UniProtKB/Swiss-Prot
-
Q9H6X4
- Related
- ENSP00000377455.3, ENST00000393877.3
- Conserved Domains (1) summary
-
- pfam05915
Location:57 → 178
- DUF872; Eukaryotic protein of unknown function (DUF872)
-
NM_001078651.3 → NP_001072119.1 transmembrane protein 134 isoform c
See identical proteins and their annotated locations for NP_001072119.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) uses an alternate in-frame splice site in the coding region, compared to variant 1. This results in a shorter protein (isoform c), compared to isoform a.
- Source sequence(s)
-
AA830850, AP003419, BC013883, HY053672, HY059123
- UniProtKB/Swiss-Prot
-
Q9H6X4
- Conserved Domains (1) summary
-
- pfam05915
Location:57 → 184
- DUF872; Eukaryotic protein of unknown function (DUF872)
-
NM_025124.4 → NP_079400.1 transmembrane protein 134 isoform a
See identical proteins and their annotated locations for NP_079400.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longest isoform (a).
- Source sequence(s)
-
AA830850, AK025402, AP003419, HY053672
- Consensus CDS
-
CCDS8167.1
- UniProtKB/Swiss-Prot
- Q08AK4, Q6PJN3, Q9H6X4
- Related
- ENSP00000312615.2, ENST00000308022.7
- Conserved Domains (1) summary
-
- pfam05915
Location:57 → 193
- DUF872; Eukaryotic protein of unknown function (DUF872)
RNA
-
NR_073409.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) uses an alternate 3' splice site, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA830850, AP003419, BC013883, HY053672
-
NR_073410.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (5) uses alternate splice sites and lacks a 3' exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA830850, AP003419, BC013883, BG719036
-
NR_073411.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (6) uses an alternate 5' splice site, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA830850, AP003419, BC013883, BM920758, HY053672
-
NR_073412.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (7) uses alternate 3' splice sites, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
BC013883, BX400047, HY053672
- Related
-
ENST00000545682.5
-
NR_073413.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (8) uses alternate 5' and 3' splice sites, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA830850, AP003419, BC013883, CN336445, HY053672