Canonical Allele Identifier: CA1591565340

Gene: GLRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151823003_151823005delinsCAG , CM000667.2:g.151823003_151823005delinsCAG	GRCh38
NC_000005.9:g.151202564_151202566delinsCAG , CM000667.1:g.151202564_151202566delinsCAG	GRCh37
NC_000005.8:g.151182757_151182759delinsCAG	NCBI36
NG_011764.1:g.106832_106834delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1060-42_1060-40delinsCTG MANE Select	ENSP00000274576.5:n.1060-42_1060-40delinsCTG
ENST00000274576.8:c.1060-42_1060-40delinsCTG	ENSP00000274576.4:n.1060-42_1060-40delinsCTG
ENST00000455880.2:c.1060-18_1060-16delinsCTG	ENSP00000411593.2:n.1060-18_1060-16delinsCTG
ENST00000462581.6:c.*818-42_*818-40delinsCTG	ENSP00000430595.1:n.*818-42_*818-40delinsCTG
NM_000171.3:c.1060-42_1060-40delinsCTG	NP_000162.2:n.1060-42_1060-40delinsCTG
NM_001146040.1:c.1060-18_1060-16delinsCTG	NP_001139512.1:n.1060-18_1060-16delinsCTG
NM_001292000.1:c.811-42_811-40delinsCTG	NP_001278929.1:n.811-42_811-40delinsCTG
NM_000171.4:c.1060-42_1060-40delinsCTG MANE Select	NP_000162.2:n.1060-42_1060-40delinsCTG
NM_001146040.2:c.1060-18_1060-16delinsCTG	NP_001139512.1:n.1060-18_1060-16delinsCTG
NM_001292000.2:c.811-42_811-40delinsCTG	NP_001278929.1:n.811-42_811-40delinsCTG