Canonical Allele Identifier: CA1591578699
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851501C= , CM000667.2:g.151851501C= GRCh38
NC_000005.9:g.151231062C= , CM000667.1:g.151231062C= GRCh37
NC_000005.8:g.151211255C= NCBI36
NG_011764.1:g.78336G=

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.801G= MANE Select ENSP00000274576.5:p.Trp267=
ENST00000274576.8:c.801G= ENSP00000274576.4:p.Trp267=
ENST00000455880.2:c.801G= ENSP00000411593.2:p.Trp267=
ENST00000462581.6:c.*559G= ENSP00000430595.1:n.*559G=
ENST00000471351.2:n.1084G=
NM_000171.3:c.801G= NP_000162.2:p.Trp267=
NM_001146040.1:c.801G= NP_001139512.1:p.Trp267=
NM_001292000.1:c.552G= NP_001278929.1:p.Trp184=
XM_005268412.2:c.801G= XP_005268469.1:p.Trp267=
NM_000171.4:c.801G= MANE Select NP_000162.2:p.Trp267=
NM_001146040.2:c.801G= NP_001139512.1:p.Trp267=
NM_001292000.2:c.552G= NP_001278929.1:p.Trp184=