Canonical Allele Identifier: CA361849960
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs764768992

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151822825A>T , CM000667.2:g.151822825A>T GRCh38
NC_000005.9:g.151202386A>T , CM000667.1:g.151202386A>T GRCh37
NC_000005.8:g.151182579A>T NCBI36
NG_011764.1:g.107012T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.1198T>A MANE Select ENSP00000274576.5:p.Ser400Thr
ENST00000274576.8:c.1198T>A ENSP00000274576.4:p.Ser400Thr
ENST00000455880.2:c.1222T>A ENSP00000411593.2:p.Ser408Thr
ENST00000462581.6:c.*956T>A ENSP00000430595.1:n.*956T>A
NM_000171.3:c.1198T>A NP_000162.2:p.Ser400Thr
NM_001146040.1:c.1222T>A NP_001139512.1:p.Ser408Thr
NM_001292000.1:c.949T>A NP_001278929.1:p.Ser317Thr
NM_000171.4:c.1198T>A MANE Select NP_000162.2:p.Ser400Thr
NM_001146040.2:c.1222T>A NP_001139512.1:p.Ser408Thr
NM_001292000.2:c.949T>A NP_001278929.1:p.Ser317Thr