Canonical Allele Identifier: CA447224734
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1316093645

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851603A>G , CM000667.2:g.151851603A>G GRCh38
NC_000005.9:g.151231164A>G , CM000667.1:g.151231164A>G GRCh37
NC_000005.8:g.151211357A>G NCBI36
NG_011764.1:g.78234T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.699T>C MANE Select ENSP00000274576.5:p.Gly233=
ENST00000274576.8:c.699T>C ENSP00000274576.4:p.Gly233=
ENST00000455880.2:c.699T>C ENSP00000411593.2:p.Gly233=
ENST00000462581.6:c.*457T>C ENSP00000430595.1:n.*457T>C
ENST00000471351.2:n.982T>C
NM_000171.3:c.699T>C NP_000162.2:p.Gly233=
NM_001146040.1:c.699T>C NP_001139512.1:p.Gly233=
NM_001292000.1:c.450T>C NP_001278929.1:p.Gly150=
XM_005268412.2:c.699T>C XP_005268469.1:p.Gly233=
NM_000171.4:c.699T>C MANE Select NP_000162.2:p.Gly233=
NM_001146040.2:c.699T>C NP_001139512.1:p.Gly233=
NM_001292000.2:c.450T>C NP_001278929.1:p.Gly150=