Canonical Allele Identifier: CA341377
Gene: GLRA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16071
ClinVar RCV Id: RCV000017449
dbSNP Id: rs121918417

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851525G>C , CM000667.2:g.151851525G>C GRCh38
NC_000005.9:g.151231086G>C , CM000667.1:g.151231086G>C GRCh37
NC_000005.8:g.151211279G>C NCBI36
NG_011764.1:g.78312C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.777C>G MANE Select ENSP00000274576.5:p.Ser259Arg
ENST00000274576.8:c.777C>G ENSP00000274576.4:p.Ser259Arg
ENST00000455880.2:c.777C>G ENSP00000411593.2:p.Ser259Arg
ENST00000462581.6:c.*535C>G ENSP00000430595.1:n.*535C>G
ENST00000471351.2:n.1060C>G
NM_000171.3:c.777C>G NP_000162.2:p.Ser259Arg
NM_001146040.1:c.777C>G NP_001139512.1:p.Ser259Arg
NM_001292000.1:c.528C>G NP_001278929.1:p.Ser176Arg
XM_005268412.2:c.777C>G XP_005268469.1:p.Ser259Arg
NM_000171.4:c.777C>G MANE Select NP_000162.2:p.Ser259Arg
NM_001146040.2:c.777C>G NP_001139512.1:p.Ser259Arg
NM_001292000.2:c.528C>G NP_001278929.1:p.Ser176Arg