Canonical Allele Identifier: CA2569816959

Gene: GRID1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848793G>T , CM000672.2:g.85848793G>T	GRCh38
NC_000010.10:g.87608550G>T , CM000672.1:g.87608550G>T	GRCh37
NC_000010.9:g.87598530G>T	NCBI36
NG_011875.1:g.522701C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327946.12:c.1233+5703C>A MANE Select	ENSP00000330148.7:n.1233+5703C>A
ENST00000327946.11:c.1233+5703C>A	ENSP00000330148.7:n.1233+5703C>A
ENST00000464741.2:c.1233+5703C>A	ENSP00000433064.1:n.1233+5703C>A
ENST00000536331.5:c.453+5703C>A	ENSP00000444455.2:n.453+5703C>A
NM_017551.2:c.1233+5703C>A	NP_060021.1:n.1233+5703C>A
XM_011539720.1:c.1233+5703C>A	XP_011538022.1:n.1233+5703C>A
XM_011539720.2:c.1233+5703C>A	XP_011538022.1:n.1233+5703C>A
NM_017551.3:c.1233+5703C>A MANE Select	NP_060021.1:n.1233+5703C>A