Canonical Allele Identifier: CA447224525
Gene: GLRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.151230972G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851411G>C , CM000667.2:g.151851411G>C GRCh38
NC_000005.9:g.151230972G>C , CM000667.1:g.151230972G>C GRCh37
NC_000005.8:g.151211165G>C NCBI36
NG_011764.1:g.78426C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.891C>G MANE Select ENSP00000274576.5:p.Gly297=
ENST00000274576.8:c.891C>G ENSP00000274576.4:p.Gly297=
ENST00000455880.2:c.891C>G ENSP00000411593.2:p.Gly297=
ENST00000462581.6:c.*649C>G ENSP00000430595.1:n.*649C>G
ENST00000471351.2:n.1174C>G
NM_000171.3:c.891C>G NP_000162.2:p.Gly297=
NM_001146040.1:c.891C>G NP_001139512.1:p.Gly297=
NM_001292000.1:c.642C>G NP_001278929.1:p.Gly214=
XM_005268412.2:c.891C>G XP_005268469.1:p.Gly297=
NM_000171.4:c.891C>G MANE Select NP_000162.2:p.Gly297=
NM_001146040.2:c.891C>G NP_001139512.1:p.Gly297=
NM_001292000.2:c.642C>G NP_001278929.1:p.Gly214=