NEW
Try the new Transcript table
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_001286990.2 → NP_001273919.1 nucleotide sugar transporter SLC35D2 isoform b
See identical proteins and their annotated locations for NP_001273919.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) lacks three alternate exons that result in the loss of an in-frame segment in the central coding region, compared to variant 1. The encoded isoform (b) is shorter than isoform a.
- Source sequence(s)
-
AL160269, BC100278, BX361048
- Consensus CDS
-
CCDS69625.1
- UniProtKB/Swiss-Prot
-
Q76EJ3
- Related
- ENSP00000364408.4, ENST00000375259.9
-
NM_007001.3 → NP_008932.2 nucleotide sugar transporter SLC35D2 isoform a
See identical proteins and their annotated locations for NP_008932.2
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (a).
- Source sequence(s)
-
AB106537, AJ005866, AL160269
- Consensus CDS
-
CCDS6717.1
- UniProtKB/Swiss-Prot
- O95454, Q498C1, Q75W21, Q76EJ3, Q7Z5X5
- Related
- ENSP00000253270.7, ENST00000253270.13
- Conserved Domains (1) summary
-
- cl26744
Location:28 → 325
- TPT; Triose-phosphate Transporter family
RNA
-
NR_104627.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) includes an alternate 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)
-
AK024841, AK307890, AL160269, BX361048, DB547513
- Related
-
ENST00000650065.1
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000009.12 Reference GRCh38.p14 Primary Assembly
- Range
-
96313444..96383711 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060933.1 Alternate T2T-CHM13v2.0
- Range
-
108485153..108555432 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)