Canonical Allele Identifier: CA1591578729
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851597G= , CM000667.2:g.151851597G= GRCh38
NC_000005.9:g.151231158G= , CM000667.1:g.151231158G= GRCh37
NC_000005.8:g.151211351G= NCBI36
NG_011764.1:g.78240C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.705C= MANE Select ENSP00000274576.5:p.Phe235=
ENST00000274576.8:c.705C= ENSP00000274576.4:p.Phe235=
ENST00000455880.2:c.705C= ENSP00000411593.2:p.Phe235=
ENST00000462581.6:c.*463C= ENSP00000430595.1:n.*463C=
ENST00000471351.2:n.988C=
NM_000171.3:c.705C= NP_000162.2:p.Phe235=
NM_001146040.1:c.705C= NP_001139512.1:p.Phe235=
NM_001292000.1:c.456C= NP_001278929.1:p.Phe152=
XM_005268412.2:c.705C= XP_005268469.1:p.Phe235=
NM_000171.4:c.705C= MANE Select NP_000162.2:p.Phe235=
NM_001146040.2:c.705C= NP_001139512.1:p.Phe235=
NM_001292000.2:c.456C= NP_001278929.1:p.Phe152=