Canonical Allele Identifier: CA13294259

Gene: GRID1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86087202C>G , CM000672.2:g.86087202C>G	GRCh38
NC_000010.10:g.87846959C>G , CM000672.1:g.87846959C>G	GRCh37
NC_000010.9:g.87836939C>G	NCBI36
NG_011875.1:g.284292G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327946.12:c.726+51617G>C MANE Select	ENSP00000330148.7:n.726+51617G>C
ENST00000327946.11:c.726+51617G>C	ENSP00000330148.7:n.726+51617G>C
ENST00000464741.2:c.726+51617G>C	ENSP00000433064.1:n.726+51617G>C
NM_017551.2:c.726+51617G>C	NP_060021.1:n.726+51617G>C
XM_011539720.1:c.726+51617G>C	XP_011538022.1:n.726+51617G>C
XM_011539720.2:c.726+51617G>C	XP_011538022.1:n.726+51617G>C
NM_017551.3:c.726+51617G>C MANE Select	NP_060021.1:n.726+51617G>C