Canonical Allele Identifier: CA12013119
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs991774172

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851329A>C , CM000667.2:g.151851329A>C GRCh38
NC_000005.9:g.151230890A>C , CM000667.1:g.151230890A>C GRCh37
NC_000005.8:g.151211083A>C NCBI36
NG_011764.1:g.78508T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.912+61T>G MANE Select ENSP00000274576.5:n.912+61T>G
ENST00000274576.8:c.912+61T>G ENSP00000274576.4:n.912+61T>G
ENST00000455880.2:c.912+61T>G ENSP00000411593.2:n.912+61T>G
ENST00000462581.6:c.*670+61T>G ENSP00000430595.1:n.*670+61T>G
ENST00000471351.2:n.1195+61T>G
NM_000171.3:c.912+61T>G NP_000162.2:n.912+61T>G
NM_001146040.1:c.912+61T>G NP_001139512.1:n.912+61T>G
NM_001292000.1:c.663+61T>G NP_001278929.1:n.663+61T>G
XM_005268412.2:c.912+61T>G XP_005268469.1:n.912+61T>G
NM_000171.4:c.912+61T>G MANE Select NP_000162.2:n.912+61T>G
NM_001146040.2:c.912+61T>G NP_001139512.1:n.912+61T>G
NM_001292000.2:c.663+61T>G NP_001278929.1:n.663+61T>G