Canonical Allele Identifier: CA1591568004
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151829006G= , CM000667.2:g.151829006G= GRCh38
NC_000005.9:g.151208567G= , CM000667.1:g.151208567G= GRCh37
NC_000005.8:g.151188760G= NCBI36
NG_011764.1:g.100831C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.974C= MANE Select ENSP00000274576.5:p.Ala325=
ENST00000274576.8:c.974C= ENSP00000274576.4:p.Ala325=
ENST00000455880.2:c.974C= ENSP00000411593.2:p.Ala325=
ENST00000462581.6:c.*732C= ENSP00000430595.1:n.*732C=
NM_000171.3:c.974C= NP_000162.2:p.Ala325=
NM_001146040.1:c.974C= NP_001139512.1:p.Ala325=
NM_001292000.1:c.725C= NP_001278929.1:p.Ala242=
NM_000171.4:c.974C= MANE Select NP_000162.2:p.Ala325=
NM_001146040.2:c.974C= NP_001139512.1:p.Ala325=
NM_001292000.2:c.725C= NP_001278929.1:p.Ala242=