Canonical Allele Identifier: CA1591578668
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851420C= , CM000667.2:g.151851420C= GRCh38
NC_000005.9:g.151230981C= , CM000667.1:g.151230981C= GRCh37
NC_000005.8:g.151211174C= NCBI36
NG_011764.1:g.78417G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.882G= MANE Select ENSP00000274576.5:p.Gln294=
ENST00000274576.8:c.882G= ENSP00000274576.4:p.Gln294=
ENST00000455880.2:c.882G= ENSP00000411593.2:p.Gln294=
ENST00000462581.6:c.*640G= ENSP00000430595.1:n.*640G=
ENST00000471351.2:n.1165G=
NM_000171.3:c.882G= NP_000162.2:p.Gln294=
NM_001146040.1:c.882G= NP_001139512.1:p.Gln294=
NM_001292000.1:c.633G= NP_001278929.1:p.Gln211=
XM_005268412.2:c.882G= XP_005268469.1:p.Gln294=
NM_000171.4:c.882G= MANE Select NP_000162.2:p.Gln294=
NM_001146040.2:c.882G= NP_001139512.1:p.Gln294=
NM_001292000.2:c.633G= NP_001278929.1:p.Gln211=