Canonical Allele Identifier: CA1591565327

Gene: GLRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822981_151822984delinsTGGG , CM000667.2:g.151822981_151822984delinsTGGG	GRCh38
NC_000005.9:g.151202542_151202545delinsTGGG , CM000667.1:g.151202542_151202545delinsTGGG	GRCh37
NC_000005.8:g.151182735_151182738delinsTGGG	NCBI36
NG_011764.1:g.106853_106856delinsCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1060-21_1060-18delinsCCCA MANE Select	ENSP00000274576.5:n.1060-21_1060-18delinsCCCA
ENST00000274576.8:c.1060-21_1060-18delinsCCCA	ENSP00000274576.4:n.1060-21_1060-18delinsCCCA
ENST00000455880.2:c.1063_1066delinsCCCA	ENSP00000411593.2:p.Pro355=
ENST00000462581.6:c.*818-21_*818-18delinsCCCA	ENSP00000430595.1:n.*818-21_*818-18delinsCCCA
NM_000171.3:c.1060-21_1060-18delinsCCCA	NP_000162.2:n.1060-21_1060-18delinsCCCA
NM_001146040.1:c.1063_1066delinsCCCA	NP_001139512.1:p.Pro355=
NM_001292000.1:c.811-21_811-18delinsCCCA	NP_001278929.1:n.811-21_811-18delinsCCCA
NM_000171.4:c.1060-21_1060-18delinsCCCA MANE Select	NP_000162.2:n.1060-21_1060-18delinsCCCA
NM_001146040.2:c.1063_1066delinsCCCA	NP_001139512.1:p.Pro355=
NM_001292000.2:c.811-21_811-18delinsCCCA	NP_001278929.1:n.811-21_811-18delinsCCCA