Human (GRCh38.p14)
Description

lipase C, hepatic type [Source:HGNC Symbol;Acc:HGNC:6619]

Gene Synonyms

HL, HTGL

Location
About this transcript

This transcript has 9 exons, is annotated with 32 domains and features, is associated with 67974 variant alleles and maps to 360 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000299022.10LIPC-2012559499aaENSP00000299022.5
 
Protein coding
CCDS10166P11150 NM_000236.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000414170.7LIPC-2032968499aaENSP00000395569.3
 
Protein coding
E7EUJ1 -GENCODE basicTSL:1
ENST00000356113.10LIPC-2022161499aaENSP00000348425.6
 
Protein coding
CCDS10166P11150 -GENCODE basicAPPRIS P1TSL:2
ENST00000433326.2LIPC-2041484438aaENSP00000395002.2
 
Protein coding
E7EUK6 -GENCODE basicTSL:2
ENST00000559845.5LIPC-2051530No protein-
 
Retained intron
--TSL:1
ENST00000560257.1LIPC-206934No protein-
 
Retained intron
--TSL:5
ENST00000560664.1LIPC-207815No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 9, Coding exons: 9, Transcript length: 2,559 bps, Translation length: 499 residues

MANE

This MANE Select transcript contains ENSP00000299022 and matches to NM_000236.3 and NP_000227.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P11150

CCDS

This transcript is a member of the Human CCDS set: CCDS10166

Transcript Support Level (TSL)

TSL:1

Version

ENST00000299022.10

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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