Canonical Allele Identifier: CA1591578681
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851457C= , CM000667.2:g.151851457C= GRCh38
NC_000005.9:g.151231018C= , CM000667.1:g.151231018C= GRCh37
NC_000005.8:g.151211211C= NCBI36
NG_011764.1:g.78380G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.845G= MANE Select ENSP00000274576.5:p.Gly282=
ENST00000274576.8:c.845G= ENSP00000274576.4:p.Gly282=
ENST00000455880.2:c.845G= ENSP00000411593.2:p.Gly282=
ENST00000462581.6:c.*603G= ENSP00000430595.1:n.*603G=
ENST00000471351.2:n.1128G=
NM_000171.3:c.845G= NP_000162.2:p.Gly282=
NM_001146040.1:c.845G= NP_001139512.1:p.Gly282=
NM_001292000.1:c.596G= NP_001278929.1:p.Gly199=
XM_005268412.2:c.845G= XP_005268469.1:p.Gly282=
NM_000171.4:c.845G= MANE Select NP_000162.2:p.Gly282=
NM_001146040.2:c.845G= NP_001139512.1:p.Gly282=
NM_001292000.2:c.596G= NP_001278929.1:p.Gly199=