Canonical Allele Identifier: CA1477204558

Gene: GRID2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.93515346C= , CM000666.2:g.93515346C=	GRCh38
NC_000004.11:g.94436497C= , CM000666.1:g.94436497C=	GRCh37
NC_000004.10:g.94655520C=	NCBI36
NG_034113.1:g.1215948C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001510.4:c.2128C= MANE Select	NP_001501.2:p.Arg710=
ENST00000282020.9:c.2128C= MANE Select	ENSP00000282020.4:p.Arg710=
NM_001286838.1:c.1843C=	NP_001273767.1:p.Arg615=
NM_001510.3:c.2128C=	NP_001501.2:p.Arg710=
ENST00000282020.8:c.2128C=	ENSP00000282020.4:p.Arg710=
ENST00000510992.5:c.1843C=	ENSP00000421257.1:p.Arg615=
ENST00000611049.4:c.1885C=	ENSP00000483084.1:p.Arg629=
XM_011531893.1:c.1999C=	XP_011530195.1:p.Arg667=
XM_011531893.2:c.2212C=	XP_011530195.2:p.Arg738=
XM_011531894.1:c.1444C=	XP_011530196.1:p.Arg482=
XM_011531894.2:c.1444C=	XP_011530196.1:p.Arg482=
XM_011531895.1:c.1219C=	XP_011530197.1:p.Arg407=
XM_011531895.2:c.1219C=	XP_011530197.1:p.Arg407=
XM_017008118.1:c.2164C=	XP_016863607.1:p.Arg722=
XM_017008119.1:c.1996C=	XP_016863608.1:p.Arg666=
XM_017008120.2:c.2212C=	XP_016863609.1:p.Arg738=
XM_017008121.1:c.2212C=	XP_016863610.1:p.Arg738=
XM_017008122.2:c.2128C=	XP_016863611.1:p.Arg710=
XM_017008123.1:c.1171C=	XP_016863612.1:p.Arg391=
XM_017008124.1:c.1171C=	XP_016863613.1:p.Arg391=
XM_017008125.1:c.1171C=	XP_016863614.1:p.Arg391=
XM_024454024.1:c.2176C=	XP_024309792.1:p.Arg726=
XM_024454025.1:c.1171C=	XP_024309793.1:p.Arg391=
XM_024454026.1:c.1129C=	XP_024309794.1:p.Arg377=