Canonical Allele Identifier: CA1591565335

Gene: GLRA1

Linked Data

• dbSNP Id: rs1763181552
• gnomAD v4: 5-151822992-TTAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822996_151823000del , CM000667.2:g.151822996_151823000del	GRCh38
NC_000005.9:g.151202557_151202561del , CM000667.1:g.151202557_151202561del	GRCh37
NC_000005.8:g.151182750_151182754del	NCBI36
NG_011764.1:g.106840_106844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1060-34_1060-30del MANE Select	ENSP00000274576.5:n.1060-34_1060-30del
ENST00000274576.8:c.1060-34_1060-30del	ENSP00000274576.4:n.1060-34_1060-30del
ENST00000455880.2:c.1060-10_1060-6del	ENSP00000411593.2:n.1060-10_1060-6del
ENST00000462581.6:c.*818-34_*818-30del	ENSP00000430595.1:n.*818-34_*818-30del
NM_000171.3:c.1060-34_1060-30del	NP_000162.2:n.1060-34_1060-30del
NM_001146040.1:c.1060-10_1060-6del	NP_001139512.1:n.1060-10_1060-6del
NM_001292000.1:c.811-34_811-30del	NP_001278929.1:n.811-34_811-30del
NM_000171.4:c.1060-34_1060-30del MANE Select	NP_000162.2:n.1060-34_1060-30del
NM_001146040.2:c.1060-10_1060-6del	NP_001139512.1:n.1060-10_1060-6del
NM_001292000.2:c.811-34_811-30del	NP_001278929.1:n.811-34_811-30del