Canonical Allele Identifier: CA210633061

Gene: GRID1

Linked Data

• dbSNP Id: rs192800617
• gnomAD v2: 10-87740794-C-G
• gnomAD v3: 10-85981037-C-G
• gnomAD v4: 10-85981037-C-G
• MyVariant Identifiers: chr10:g.87740794C>G (hg19) ; chr10:g.85981037C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85981037C>G , CM000672.2:g.85981037C>G	GRCh38
NC_000010.10:g.87740794C>G , CM000672.1:g.87740794C>G	GRCh37
NC_000010.9:g.87730774C>G	NCBI36
NG_011875.1:g.390457G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.727-64798G>C MANE Select	ENSP00000330148.7:n.727-64798G>C
ENST00000327946.11:c.727-64798G>C	ENSP00000330148.7:n.727-64798G>C
ENST00000464741.2:c.727-64798G>C	ENSP00000433064.1:n.727-64798G>C
NM_017551.2:c.727-64798G>C	NP_060021.1:n.727-64798G>C
XM_011539720.1:c.727-64798G>C	XP_011538022.1:n.727-64798G>C
XM_011539720.2:c.727-64798G>C	XP_011538022.1:n.727-64798G>C
NM_017551.3:c.727-64798G>C MANE Select	NP_060021.1:n.727-64798G>C