Canonical Allele Identifier: CA361850452

Gene: GLRA1

Linked Data

• dbSNP Id: rs1554081983
• MyVariant Identifiers: chr5:g.151202566_151202567del (hg19) ; chr5:g.151823006_151823007del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151823007_151823008del , CM000667.2:g.151823007_151823008del	GRCh38
NC_000005.9:g.151202568_151202569del , CM000667.1:g.151202568_151202569del	GRCh37
NC_000005.8:g.151182761_151182762del	NCBI36
NG_011764.1:g.106831_106832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1060-43_1060-42del MANE Select	ENSP00000274576.5:n.1060-43_1060-42del
ENST00000274576.8:c.1060-43_1060-42del	ENSP00000274576.4:n.1060-43_1060-42del
ENST00000455880.2:c.1060-19_1060-18del	ENSP00000411593.2:n.1060-19_1060-18del
ENST00000462581.6:c.*818-43_*818-42del	ENSP00000430595.1:n.*818-43_*818-42del
NM_000171.3:c.1060-43_1060-42del	NP_000162.2:n.1060-43_1060-42del
NM_001146040.1:c.1060-19_1060-18del	NP_001139512.1:n.1060-19_1060-18del
NM_001292000.1:c.811-43_811-42del	NP_001278929.1:n.811-43_811-42del
NM_000171.4:c.1060-43_1060-42del MANE Select	NP_000162.2:n.1060-43_1060-42del
NM_001146040.2:c.1060-19_1060-18del	NP_001139512.1:n.1060-19_1060-18del
NM_001292000.2:c.811-43_811-42del	NP_001278929.1:n.811-43_811-42del