Canonical Allele Identifier: CA1591568051
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151829091_151829093delinsCAG , CM000667.2:g.151829091_151829093delinsCAG GRCh38
NC_000005.9:g.151208652_151208654delinsCAG , CM000667.1:g.151208652_151208654delinsCAG GRCh37
NC_000005.8:g.151188845_151188847delinsCAG NCBI36
NG_011764.1:g.100744_100746delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.913-26_913-24delinsCTG MANE Select ENSP00000274576.5:n.913-26_913-24delinsCTG
ENST00000274576.8:c.913-26_913-24delinsCTG ENSP00000274576.4:n.913-26_913-24delinsCTG
ENST00000455880.2:c.913-26_913-24delinsCTG ENSP00000411593.2:n.913-26_913-24delinsCTG
ENST00000462581.6:c.*671-26_*671-24delinsCTG ENSP00000430595.1:n.*671-26_*671-24delinsCTG
NM_000171.3:c.913-26_913-24delinsCTG NP_000162.2:n.913-26_913-24delinsCTG
NM_001146040.1:c.913-26_913-24delinsCTG NP_001139512.1:n.913-26_913-24delinsCTG
NM_001292000.1:c.664-26_664-24delinsCTG NP_001278929.1:n.664-26_664-24delinsCTG
NM_000171.4:c.913-26_913-24delinsCTG MANE Select NP_000162.2:n.913-26_913-24delinsCTG
NM_001146040.2:c.913-26_913-24delinsCTG NP_001139512.1:n.913-26_913-24delinsCTG
NM_001292000.2:c.664-26_664-24delinsCTG NP_001278929.1:n.664-26_664-24delinsCTG