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Human (GRCh37.p13)
Description

hydrolethalus syndrome 1 [Source:HGNC Symbol;Acc:26558]

Gene Synonyms

FLJ32915, HLS

About this transcript

This transcript has 3 exons, is annotated with 10 domains and features, is associated with 6043 variant alleles and maps to 255 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000425380.2HYLS1-0022061299aaENSP00000414884.2
 
Protein coding
CCDS8467Q96M11 NM_001134793.1Ensembl CanonicalGENCODE basic
ENST00000356438.3HYLS1-0011810299aaENSP00000348815.3
 
Protein coding
CCDS8467Q96M11 NM_145014.2GENCODE basic
ENST00000526028.1HYLS1-0031803299aaENSP00000436833.1
 
Protein coding
CCDS8467Q96M11 -GENCODE basic
Statistics

Exons: 3, Coding exons: 1, Transcript length: 1,803 bps, Translation length: 299 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96M11

CCDS

This transcript is a member of the Human CCDS set: CCDS8467

Version

ENST00000526028.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000386734 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.