Canonical Allele Identifier: CA1591565216
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151822764C= , CM000667.2:g.151822764C= GRCh38
NC_000005.9:g.151202325C= , CM000667.1:g.151202325C= GRCh37
NC_000005.8:g.151182518C= NCBI36
NG_011764.1:g.107073G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1259G= MANE Select ENSP00000274576.5:p.Arg420=
ENST00000274576.8:c.1259G= ENSP00000274576.4:p.Arg420=
ENST00000455880.2:c.1283G= ENSP00000411593.2:p.Arg428=
ENST00000462581.6:c.*1017G= ENSP00000430595.1:n.*1017G=
NM_000171.3:c.1259G= NP_000162.2:p.Arg420=
NM_001146040.1:c.1283G= NP_001139512.1:p.Arg428=
NM_001292000.1:c.1010G= NP_001278929.1:p.Arg337=
NM_000171.4:c.1259G= MANE Select NP_000162.2:p.Arg420=
NM_001146040.2:c.1283G= NP_001139512.1:p.Arg428=
NM_001292000.2:c.1010G= NP_001278929.1:p.Arg337=