Canonical Allele Identifier: CA1591565231
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151822799G= , CM000667.2:g.151822799G= GRCh38
NC_000005.9:g.151202360G= , CM000667.1:g.151202360G= GRCh37
NC_000005.8:g.151182553G= NCBI36
NG_011764.1:g.107038C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1224C= MANE Select ENSP00000274576.5:p.Phe408=
ENST00000274576.8:c.1224C= ENSP00000274576.4:p.Phe408=
ENST00000455880.2:c.1248C= ENSP00000411593.2:p.Phe416=
ENST00000462581.6:c.*982C= ENSP00000430595.1:n.*982C=
NM_000171.3:c.1224C= NP_000162.2:p.Phe408=
NM_001146040.1:c.1248C= NP_001139512.1:p.Phe416=
NM_001292000.1:c.975C= NP_001278929.1:p.Phe325=
NM_000171.4:c.1224C= MANE Select NP_000162.2:p.Phe408=
NM_001146040.2:c.1248C= NP_001139512.1:p.Phe416=
NM_001292000.2:c.975C= NP_001278929.1:p.Phe325=