Canonical Allele Identifier: CA669424941

Gene: GRID1

Linked Data

• dbSNP Id: rs1428499632
• gnomAD v3: 10-86169283-G-A
• gnomAD v4: 10-86169283-G-A
• MyVariant Identifiers: chr10:g.87929040G>A (hg19) ; chr10:g.86169283G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86169283G>A , CM000672.2:g.86169283G>A	GRCh38
NC_000010.10:g.87929040G>A , CM000672.1:g.87929040G>A	GRCh37
NC_000010.9:g.87919020G>A	NCBI36
NG_011875.1:g.202211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327946.12:c.521-30259C>T MANE Select	ENSP00000330148.7:n.521-30259C>T
ENST00000327946.11:c.521-30259C>T	ENSP00000330148.7:n.521-30259C>T
ENST00000464741.2:c.521-30259C>T	ENSP00000433064.1:n.521-30259C>T
NM_017551.2:c.521-30259C>T	NP_060021.1:n.521-30259C>T
XM_011539720.1:c.521-30259C>T	XP_011538022.1:n.521-30259C>T
XM_011539720.2:c.521-30259C>T	XP_011538022.1:n.521-30259C>T
NM_017551.3:c.521-30259C>T MANE Select	NP_060021.1:n.521-30259C>T