Canonical Allele Identifier: CA1591565343

Gene: GLRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151823004_151823006delinsAGG , CM000667.2:g.151823004_151823006delinsAGG	GRCh38
NC_000005.9:g.151202565_151202567delinsAGG , CM000667.1:g.151202565_151202567delinsAGG	GRCh37
NC_000005.8:g.151182758_151182760delinsAGG	NCBI36
NG_011764.1:g.106831_106833delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1060-43_1060-41delinsCCT MANE Select	ENSP00000274576.5:n.1060-43_1060-41delinsCCT
ENST00000274576.8:c.1060-43_1060-41delinsCCT	ENSP00000274576.4:n.1060-43_1060-41delinsCCT
ENST00000455880.2:c.1060-19_1060-17delinsCCT	ENSP00000411593.2:n.1060-19_1060-17delinsCCT
ENST00000462581.6:c.*818-43_*818-41delinsCCT	ENSP00000430595.1:n.*818-43_*818-41delinsCCT
NM_000171.3:c.1060-43_1060-41delinsCCT	NP_000162.2:n.1060-43_1060-41delinsCCT
NM_001146040.1:c.1060-19_1060-17delinsCCT	NP_001139512.1:n.1060-19_1060-17delinsCCT
NM_001292000.1:c.811-43_811-41delinsCCT	NP_001278929.1:n.811-43_811-41delinsCCT
NM_000171.4:c.1060-43_1060-41delinsCCT MANE Select	NP_000162.2:n.1060-43_1060-41delinsCCT
NM_001146040.2:c.1060-19_1060-17delinsCCT	NP_001139512.1:n.1060-19_1060-17delinsCCT
NM_001292000.2:c.811-43_811-41delinsCCT	NP_001278929.1:n.811-43_811-41delinsCCT