Canonical Allele Identifier: CA1591582307
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151859968T= , CM000667.2:g.151859968T= GRCh38
NC_000005.9:g.151239529T= , CM000667.1:g.151239529T= GRCh37
NC_000005.8:g.151219722T= NCBI36
NG_011764.1:g.69869A=

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.293A= MANE Select ENSP00000274576.5:p.Asp98=
ENST00000274576.8:c.293A= ENSP00000274576.4:p.Asp98=
ENST00000455880.2:c.293A= ENSP00000411593.2:p.Asp98=
ENST00000462581.6:c.*51A= ENSP00000430595.1:n.*51A=
ENST00000471351.2:n.576A=
NM_000171.3:c.293A= NP_000162.2:p.Asp98=
NM_001146040.1:c.293A= NP_001139512.1:p.Asp98=
NM_001292000.1:c.44A= NP_001278929.1:p.Asp15=
XM_005268412.2:c.293A= XP_005268469.1:p.Asp98=
XR_002956230.1:n.229+2075T=
NM_000171.4:c.293A= MANE Select NP_000162.2:p.Asp98=
NM_001146040.2:c.293A= NP_001139512.1:p.Asp98=
NM_001292000.2:c.44A= NP_001278929.1:p.Asp15=