Canonical Allele Identifier: CA1925358898

Gene: GRID1

Linked Data

• dbSNP Id: rs1844721179

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86124369G>A , CM000672.2:g.86124369G>A	GRCh38
NC_000010.10:g.87884126G>A , CM000672.1:g.87884126G>A	GRCh37
NC_000010.9:g.87874106G>A	NCBI36
NG_011875.1:g.247125C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.726+14450C>T MANE Select	ENSP00000330148.7:n.726+14450C>T
ENST00000327946.11:c.726+14450C>T	ENSP00000330148.7:n.726+14450C>T
ENST00000464741.2:c.726+14450C>T	ENSP00000433064.1:n.726+14450C>T
NM_017551.2:c.726+14450C>T	NP_060021.1:n.726+14450C>T
XM_011539720.1:c.726+14450C>T	XP_011538022.1:n.726+14450C>T
XM_011539720.2:c.726+14450C>T	XP_011538022.1:n.726+14450C>T
NM_017551.3:c.726+14450C>T MANE Select	NP_060021.1:n.726+14450C>T