Canonical Allele Identifier: CA357724777

Gene: GRID2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.93490725A>G , CM000666.2:g.93490725A>G	GRCh38
NC_000004.11:g.94411876A>G , CM000666.1:g.94411876A>G	GRCh37
NC_000004.10:g.94630899A>G	NCBI36
NG_034113.1:g.1191327A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001510.4:c.1945A>G MANE Select	NP_001501.2:p.Thr649Ala
ENST00000282020.9:c.1945A>G MANE Select	ENSP00000282020.4:p.Thr649Ala
NM_001286838.1:c.1660A>G	NP_001273767.1:p.Thr554Ala
NM_001510.3:c.1945A>G	NP_001501.2:p.Thr649Ala
ENST00000282020.8:c.1945A>G	ENSP00000282020.4:p.Thr649Ala
ENST00000510992.5:c.1660A>G	ENSP00000421257.1:p.Thr554Ala
ENST00000611049.4:c.1702A>G	ENSP00000483084.1:p.Thr568Ala
XM_011531893.1:c.1816A>G	XP_011530195.1:p.Thr606Ala
XM_011531893.2:c.2029A>G	XP_011530195.2:p.Thr677Ala
XM_011531894.1:c.1261A>G	XP_011530196.1:p.Thr421Ala
XM_011531894.2:c.1261A>G	XP_011530196.1:p.Thr421Ala
XM_011531895.1:c.1036A>G	XP_011530197.1:p.Thr346Ala
XM_011531895.2:c.1036A>G	XP_011530197.1:p.Thr346Ala
XM_017008118.1:c.1981A>G	XP_016863607.1:p.Thr661Ala
XM_017008119.1:c.1813A>G	XP_016863608.1:p.Thr605Ala
XM_017008120.2:c.2029A>G	XP_016863609.1:p.Thr677Ala
XM_017008121.1:c.2029A>G	XP_016863610.1:p.Thr677Ala
XM_017008122.2:c.1945A>G	XP_016863611.1:p.Thr649Ala
XM_017008123.1:c.988A>G	XP_016863612.1:p.Thr330Ala
XM_017008124.1:c.988A>G	XP_016863613.1:p.Thr330Ala
XM_017008125.1:c.988A>G	XP_016863614.1:p.Thr330Ala
XM_024454024.1:c.1993A>G	XP_024309792.1:p.Thr665Ala
XM_024454025.1:c.988A>G	XP_024309793.1:p.Thr330Ala
XM_024454026.1:c.946A>G	XP_024309794.1:p.Thr316Ala