Canonical Allele Identifier: CA1591565347

Gene: GLRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151823014_151823015delinsCA , CM000667.2:g.151823014_151823015delinsCA	GRCh38
NC_000005.9:g.151202575_151202576delinsCA , CM000667.1:g.151202575_151202576delinsCA	GRCh37
NC_000005.8:g.151182768_151182769delinsCA	NCBI36
NG_011764.1:g.106822_106823delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1060-52_1060-51delinsTG MANE Select	ENSP00000274576.5:n.1060-52_1060-51delinsTG
ENST00000274576.8:c.1060-52_1060-51delinsTG	ENSP00000274576.4:n.1060-52_1060-51delinsTG
ENST00000455880.2:c.1060-28_1060-27delinsTG	ENSP00000411593.2:n.1060-28_1060-27delinsTG
ENST00000462581.6:c.*818-52_*818-51delinsTG	ENSP00000430595.1:n.*818-52_*818-51delinsTG
NM_000171.3:c.1060-52_1060-51delinsTG	NP_000162.2:n.1060-52_1060-51delinsTG
NM_001146040.1:c.1060-28_1060-27delinsTG	NP_001139512.1:n.1060-28_1060-27delinsTG
NM_001292000.1:c.811-52_811-51delinsTG	NP_001278929.1:n.811-52_811-51delinsTG
NM_000171.4:c.1060-52_1060-51delinsTG MANE Select	NP_000162.2:n.1060-52_1060-51delinsTG
NM_001146040.2:c.1060-28_1060-27delinsTG	NP_001139512.1:n.1060-28_1060-27delinsTG
NM_001292000.2:c.811-52_811-51delinsTG	NP_001278929.1:n.811-52_811-51delinsTG