Human (GRCh38.p14)
Description

G protein subunit alpha L [Source:HGNC Symbol;Acc:HGNC:4388]

Location

Chromosome 18: 11,689,264-11,885,685 forward strand.

GRCh38:CM000680.2

About this gene

This gene has 10 transcripts (splice variants), 218 orthologues, 15 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000334049.11GNAL-2026227458aaENSP00000334051.5
 
Protein coding
CCDS11851P38405-2 NM_182978.4MANE SelectEnsembl CanonicalGENCODE basicTSL:1
ENST00000423027.8GNAL-2036045381aaENSP00000408489.2
 
Protein coding
CCDS11852P38405-1 NM_001369387.1MANE Plus ClinicalGENCODE basicAPPRIS P1TSL:1
ENST00000269162.9GNAL-2011722381aaENSP00000269162.4
 
Protein coding
CCDS11852P38405-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000535121.5GNAL-2041285381aaENSP00000439023.1
 
Protein coding
CCDS11852P38405-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000602628.1GNAL-2101038174aaENSP00000473600.1
 
Protein coding
CCDS58614P38405-3 -GENCODE basicTSL:2
ENST00000585642.5GNAL-206623179aaENSP00000467345.1
 
Protein coding
K7EPE2 -TSL:4CDS 3' incomplete
ENST00000590228.1GNAL-208585145aaENSP00000467709.1
 
Protein coding
K7EQ80 -TSL:4CDS 3' incomplete
ENST00000586926.1GNAL-20745154aaENSP00000466709.1
 
Protein coding
K7EMY6 -TSL:2CDS 5' incomplete
ENST00000590972.1GNAL-209477No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000585590.1GNAL-205471No protein-
 
Protein coding CDS not defined
--TSL:2