Canonical Allele Identifier: CA1591578717
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851565C= , CM000667.2:g.151851565C= GRCh38
NC_000005.9:g.151231126C= , CM000667.1:g.151231126C= GRCh37
NC_000005.8:g.151211319C= NCBI36
NG_011764.1:g.78272G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.737G= MANE Select ENSP00000274576.5:p.Arg246=
ENST00000274576.8:c.737G= ENSP00000274576.4:p.Arg246=
ENST00000455880.2:c.737G= ENSP00000411593.2:p.Arg246=
ENST00000462581.6:c.*495G= ENSP00000430595.1:n.*495G=
ENST00000471351.2:n.1020G=
NM_000171.3:c.737G= NP_000162.2:p.Arg246=
NM_001146040.1:c.737G= NP_001139512.1:p.Arg246=
NM_001292000.1:c.488G= NP_001278929.1:p.Arg163=
XM_005268412.2:c.737G= XP_005268469.1:p.Arg246=
NM_000171.4:c.737G= MANE Select NP_000162.2:p.Arg246=
NM_001146040.2:c.737G= NP_001139512.1:p.Arg246=
NM_001292000.2:c.488G= NP_001278929.1:p.Arg163=