Canonical Allele Identifier: CA1591596304
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151892356C= , CM000667.2:g.151892356C= GRCh38
NC_000005.9:g.151271917C= , CM000667.1:g.151271917C= GRCh37
NC_000005.8:g.151252110C= NCBI36
NG_011764.1:g.37481G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.139G= MANE Select ENSP00000274576.5:p.Gly47=
ENST00000274576.8:c.139G= ENSP00000274576.4:p.Gly47=
ENST00000455880.2:c.139G= ENSP00000411593.2:p.Gly47=
ENST00000462581.6:c.57-5568G= ENSP00000430595.1:n.57-5568G=
ENST00000471351.2:n.422G=
NM_000171.3:c.139G= NP_000162.2:p.Gly47=
NM_001146040.1:c.139G= NP_001139512.1:p.Gly47=
NM_001292000.1:c.-65-5568G= NP_001278929.1:n.-65-5568G=
XM_005268412.2:c.139G= XP_005268469.1:p.Gly47=
XR_002956230.1:n.3260C=
NM_000171.4:c.139G= MANE Select NP_000162.2:p.Gly47=
NM_001146040.2:c.139G= NP_001139512.1:p.Gly47=
NM_001292000.2:c.-65-5568G= NP_001278929.1:n.-65-5568G=