Canonical Allele Identifier: CA595017963

Gene: GRID1

Linked Data

• dbSNP Id: rs1268924043
• gnomAD v2: 10-87608513-G-T
• gnomAD v3: 10-85848756-G-T
• gnomAD v4: 10-85848756-G-T
• MyVariant Identifiers: chr10:g.87608513G>T (hg19) ; chr10:g.85848756G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848756G>T , CM000672.2:g.85848756G>T	GRCh38
NC_000010.10:g.87608513G>T , CM000672.1:g.87608513G>T	GRCh37
NC_000010.9:g.87598493G>T	NCBI36
NG_011875.1:g.522738C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5740C>A MANE Select	ENSP00000330148.7:n.1233+5740C>A
ENST00000327946.11:c.1233+5740C>A	ENSP00000330148.7:n.1233+5740C>A
ENST00000464741.2:c.1233+5740C>A	ENSP00000433064.1:n.1233+5740C>A
ENST00000536331.5:c.453+5740C>A	ENSP00000444455.2:n.453+5740C>A
NM_017551.2:c.1233+5740C>A	NP_060021.1:n.1233+5740C>A
XM_011539720.1:c.1233+5740C>A	XP_011538022.1:n.1233+5740C>A
XM_011539720.2:c.1233+5740C>A	XP_011538022.1:n.1233+5740C>A
NM_017551.3:c.1233+5740C>A MANE Select	NP_060021.1:n.1233+5740C>A