Canonical Allele Identifier: CA1591578662
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851408A= , CM000667.2:g.151851408A= GRCh38
NC_000005.9:g.151230969A= , CM000667.1:g.151230969A= GRCh37
NC_000005.8:g.151211162A= NCBI36
NG_011764.1:g.78429T=

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.894T= MANE Select ENSP00000274576.5:p.Ser298=
ENST00000274576.8:c.894T= ENSP00000274576.4:p.Ser298=
ENST00000455880.2:c.894T= ENSP00000411593.2:p.Ser298=
ENST00000462581.6:c.*652T= ENSP00000430595.1:n.*652T=
ENST00000471351.2:n.1177T=
NM_000171.3:c.894T= NP_000162.2:p.Ser298=
NM_001146040.1:c.894T= NP_001139512.1:p.Ser298=
NM_001292000.1:c.645T= NP_001278929.1:p.Ser215=
XM_005268412.2:c.894T= XP_005268469.1:p.Ser298=
NM_000171.4:c.894T= MANE Select NP_000162.2:p.Ser298=
NM_001146040.2:c.894T= NP_001139512.1:p.Ser298=
NM_001292000.2:c.645T= NP_001278929.1:p.Ser215=