Canonical Allele Identifier: CA1925294373

Gene: GRID1

Linked Data

• dbSNP Id: rs1842536671
• gnomAD v3: 10-85980901-CA-C
• gnomAD v4: 10-85980901-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85980902del , CM000672.2:g.85980902del	GRCh38
NC_000010.10:g.87740659del , CM000672.1:g.87740659del	GRCh37
NC_000010.9:g.87730639del	NCBI36
NG_011875.1:g.390592del

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.727-64663del MANE Select	ENSP00000330148.7:n.727-64663del
ENST00000327946.11:c.727-64663del	ENSP00000330148.7:n.727-64663del
ENST00000464741.2:c.727-64663del	ENSP00000433064.1:n.727-64663del
NM_017551.2:c.727-64663del	NP_060021.1:n.727-64663del
XM_011539720.1:c.727-64663del	XP_011538022.1:n.727-64663del
XM_011539720.2:c.727-64663del	XP_011538022.1:n.727-64663del
NM_017551.3:c.727-64663del MANE Select	NP_060021.1:n.727-64663del