Canonical Allele Identifier: CA1925358902

Gene: GRID1

Linked Data

• dbSNP Id: rs1844721257

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86124373T>C , CM000672.2:g.86124373T>C	GRCh38
NC_000010.10:g.87884130T>C , CM000672.1:g.87884130T>C	GRCh37
NC_000010.9:g.87874110T>C	NCBI36
NG_011875.1:g.247121A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.726+14446A>G MANE Select	ENSP00000330148.7:n.726+14446A>G
ENST00000327946.11:c.726+14446A>G	ENSP00000330148.7:n.726+14446A>G
ENST00000464741.2:c.726+14446A>G	ENSP00000433064.1:n.726+14446A>G
NM_017551.2:c.726+14446A>G	NP_060021.1:n.726+14446A>G
XM_011539720.1:c.726+14446A>G	XP_011538022.1:n.726+14446A>G
XM_011539720.2:c.726+14446A>G	XP_011538022.1:n.726+14446A>G
NM_017551.3:c.726+14446A>G MANE Select	NP_060021.1:n.726+14446A>G