Canonical Allele Identifier: CA1591578645
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851370T= , CM000667.2:g.151851370T= GRCh38
NC_000005.9:g.151230931T= , CM000667.1:g.151230931T= GRCh37
NC_000005.8:g.151211124T= NCBI36
NG_011764.1:g.78467A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.912+20A= MANE Select ENSP00000274576.5:n.912+20A=
ENST00000274576.8:c.912+20A= ENSP00000274576.4:n.912+20A=
ENST00000455880.2:c.912+20A= ENSP00000411593.2:n.912+20A=
ENST00000462581.6:c.*670+20A= ENSP00000430595.1:n.*670+20A=
ENST00000471351.2:n.1195+20A=
NM_000171.3:c.912+20A= NP_000162.2:n.912+20A=
NM_001146040.1:c.912+20A= NP_001139512.1:n.912+20A=
NM_001292000.1:c.663+20A= NP_001278929.1:n.663+20A=
XM_005268412.2:c.912+20A= XP_005268469.1:n.912+20A=
NM_000171.4:c.912+20A= MANE Select NP_000162.2:n.912+20A=
NM_001146040.2:c.912+20A= NP_001139512.1:n.912+20A=
NM_001292000.2:c.663+20A= NP_001278929.1:n.663+20A=