Canonical Allele Identifier: CA2534816822

Gene: GRID1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86124279C>T , CM000672.2:g.86124279C>T	GRCh38
NC_000010.10:g.87884036C>T , CM000672.1:g.87884036C>T	GRCh37
NC_000010.9:g.87874016C>T	NCBI36
NG_011875.1:g.247215G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.726+14540G>A MANE Select	ENSP00000330148.7:n.726+14540G>A
ENST00000327946.11:c.726+14540G>A	ENSP00000330148.7:n.726+14540G>A
ENST00000464741.2:c.726+14540G>A	ENSP00000433064.1:n.726+14540G>A
NM_017551.2:c.726+14540G>A	NP_060021.1:n.726+14540G>A
XM_011539720.1:c.726+14540G>A	XP_011538022.1:n.726+14540G>A
XM_011539720.2:c.726+14540G>A	XP_011538022.1:n.726+14540G>A
NM_017551.3:c.726+14540G>A MANE Select	NP_060021.1:n.726+14540G>A