Canonical Allele Identifier: CA210601552

Gene: GRID1

Linked Data

• dbSNP Id: rs770795031
• MyVariant Identifiers: chr10:g.87608404C>A (hg19) ; chr10:g.85848647C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848647C>A , CM000672.2:g.85848647C>A	GRCh38
NC_000010.10:g.87608404C>A , CM000672.1:g.87608404C>A	GRCh37
NC_000010.9:g.87598384C>A	NCBI36
NG_011875.1:g.522847G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5849G>T MANE Select	ENSP00000330148.7:n.1233+5849G>T
ENST00000327946.11:c.1233+5849G>T	ENSP00000330148.7:n.1233+5849G>T
ENST00000464741.2:c.1233+5849G>T	ENSP00000433064.1:n.1233+5849G>T
ENST00000536331.5:c.453+5849G>T	ENSP00000444455.2:n.453+5849G>T
NM_017551.2:c.1233+5849G>T	NP_060021.1:n.1233+5849G>T
XM_011539720.1:c.1233+5849G>T	XP_011538022.1:n.1233+5849G>T
XM_011539720.2:c.1233+5849G>T	XP_011538022.1:n.1233+5849G>T
NM_017551.3:c.1233+5849G>T MANE Select	NP_060021.1:n.1233+5849G>T