Canonical Allele Identifier: CA210604430

Gene: GRID1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85875167C>T , CM000672.2:g.85875167C>T	GRCh38
NC_000010.10:g.87634924C>T , CM000672.1:g.87634924C>T	GRCh37
NC_000010.9:g.87624904C>T	NCBI36
NG_011875.1:g.496327G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327946.12:c.781-5987G>A MANE Select	ENSP00000330148.7:n.781-5987G>A
ENST00000327946.11:c.781-5987G>A	ENSP00000330148.7:n.781-5987G>A
ENST00000464741.2:c.781-5987G>A	ENSP00000433064.1:n.781-5987G>A
ENST00000536331.5:c.1-5987G>A	ENSP00000444455.2:n.1-5987G>A
NM_017551.2:c.781-5987G>A	NP_060021.1:n.781-5987G>A
XM_011539720.1:c.781-5987G>A	XP_011538022.1:n.781-5987G>A
XM_011539720.2:c.781-5987G>A	XP_011538022.1:n.781-5987G>A
NM_017551.3:c.781-5987G>A MANE Select	NP_060021.1:n.781-5987G>A