Canonical Allele Identifier: CA357722234

Gene: GRID2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.93110786C>T , CM000666.2:g.93110786C>T	GRCh38
NC_000004.11:g.94031937C>T , CM000666.1:g.94031937C>T	GRCh37
NC_000004.10:g.94250960C>T	NCBI36
NG_034113.1:g.811388C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282020.9:c.568C>T MANE Select	ENSP00000282020.4:p.Gln190Ter
ENST00000282020.8:c.568C>T	ENSP00000282020.4:p.Gln190Ter
ENST00000502699.5:c.313C>T	ENSP00000422845.1:p.Gln105Ter
ENST00000505687.5:n.740C>T
ENST00000510992.5:c.283C>T	ENSP00000421257.1:p.Gln95Ter
ENST00000515744.5:n.398C>T
ENST00000611049.4:c.325C>T	ENSP00000483084.1:p.Gln109Ter
NM_001286838.1:c.283C>T	NP_001273767.1:p.Gln95Ter
NM_001510.3:c.568C>T	NP_001501.2:p.Gln190Ter
XM_011531893.1:c.391C>T	XP_011530195.1:p.Gln131Ter
XM_011531893.2:c.604C>T	XP_011530195.2:p.Gln202Ter
XM_017008118.1:c.604C>T	XP_016863607.1:p.Gln202Ter
XM_017008119.1:c.388C>T	XP_016863608.1:p.Gln130Ter
XM_017008120.2:c.604C>T	XP_016863609.1:p.Gln202Ter
XM_017008121.1:c.604C>T	XP_016863610.1:p.Gln202Ter
XM_017008122.2:c.568C>T	XP_016863611.1:p.Gln190Ter
XM_017008127.1:c.604C>T	XP_016863616.1:p.Gln202Ter
XM_024454024.1:c.568C>T	XP_024309792.1:p.Gln190Ter
NM_001510.4:c.568C>T MANE Select	NP_001501.2:p.Gln190Ter