Canonical Allele Identifier: CA210700043

Gene: GRID1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86232159C>T , CM000672.2:g.86232159C>T	GRCh38
NC_000010.10:g.87991916C>T , CM000672.1:g.87991916C>T	GRCh37
NC_000010.9:g.87981896C>T	NCBI36
NG_011875.1:g.139335G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327946.12:c.236-25511G>A MANE Select	ENSP00000330148.7:n.236-25511G>A
ENST00000327946.11:c.236-25511G>A	ENSP00000330148.7:n.236-25511G>A
ENST00000464741.2:c.236-25511G>A	ENSP00000433064.1:n.236-25511G>A
NM_017551.2:c.236-25511G>A	NP_060021.1:n.236-25511G>A
XM_011539720.1:c.236-25511G>A	XP_011538022.1:n.236-25511G>A
XM_011539720.2:c.236-25511G>A	XP_011538022.1:n.236-25511G>A
NM_017551.3:c.236-25511G>A MANE Select	NP_060021.1:n.236-25511G>A