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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_001411112.1 → NP_001398041.1 pleckstrin homology domain-containing family H member 3 isoform 2 precursor
Status: VALIDATED
- Source sequence(s)
-
AC067852
- Consensus CDS
-
CCDS92327.1
- UniProtKB/TrEMBL
-
X6R3U4
- Related
- ENSP00000293349.6, ENST00000293349.10
-
NM_024927.5 → NP_079203.4 pleckstrin homology domain-containing family H member 3 isoform 1 precursor
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) represents the longest transcript and encodes the supported protein.
- Source sequence(s)
-
AC067852
- Consensus CDS
-
CCDS11434.1
- UniProtKB/Swiss-Prot
- C9JQ76, Q59H20, Q7Z736, Q96B28, Q9H7D6, Q9NT18
- Related
- ENSP00000468678.1, ENST00000591022.6
- Conserved Domains (4) summary
-
- cd13297
Location:84 → 208
- PH3_MyoX-like; Myosin X-like Pleckstrin homology (PH) domain, repeat 3
- pfam00784
Location:286 → 397
- MyTH4; MyTH4 domain
- cl09511
Location:406 → 563
- FERM_B-lobe; FERM domain B-lobe
- cl17171
Location:660 → 747
- PH-like; Pleckstrin homology-like domain
RNA
-
NR_073573.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) uses an alternate splice site in an internal 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)
-
AC067852
-
NR_073574.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) contains an alternate 5' terminal exon and uses alternate splice sites in internal exons, compared to variant 1. This variant is represented as non-coding because it lacks a large portion of the coding region, including the translational start codon, found in variant 1.
- Source sequence(s)
-
AC067852
- Related
-
ENST00000456950.6