Canonical Allele Identifier: CA1591565389
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151823104G= , CM000667.2:g.151823104G= GRCh38
NC_000005.9:g.151202665G= , CM000667.1:g.151202665G= GRCh37
NC_000005.8:g.151182858G= NCBI36
NG_011764.1:g.106733C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1060-141C= MANE Select ENSP00000274576.5:n.1060-141C=
ENST00000274576.8:c.1060-141C= ENSP00000274576.4:n.1060-141C=
ENST00000455880.2:c.1060-117C= ENSP00000411593.2:n.1060-117C=
ENST00000462581.6:c.*818-141C= ENSP00000430595.1:n.*818-141C=
NM_000171.3:c.1060-141C= NP_000162.2:n.1060-141C=
NM_001146040.1:c.1060-117C= NP_001139512.1:n.1060-117C=
NM_001292000.1:c.811-141C= NP_001278929.1:n.811-141C=
NM_000171.4:c.1060-141C= MANE Select NP_000162.2:n.1060-141C=
NM_001146040.2:c.1060-117C= NP_001139512.1:n.1060-117C=
NM_001292000.2:c.811-141C= NP_001278929.1:n.811-141C=