Canonical Allele Identifier: CA1477179579

Gene: GRID2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.93461245C= , CM000666.2:g.93461245C=	GRCh38
NC_000004.11:g.94382396C= , CM000666.1:g.94382396C=	GRCh37
NC_000004.10:g.94601419C=	NCBI36
NG_034113.1:g.1161847C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001510.4:c.1858+5271C= MANE Select	NP_001501.2:n.1858+5271C=
ENST00000282020.9:c.1858+5271C= MANE Select	ENSP00000282020.4:n.1858+5271C=
NM_001286838.1:c.1573+5271C=	NP_001273767.1:n.1573+5271C=
NM_001510.3:c.1858+5271C=	NP_001501.2:n.1858+5271C=
ENST00000282020.8:c.1858+5271C=	ENSP00000282020.4:n.1858+5271C=
ENST00000510992.5:c.1573+5271C=	ENSP00000421257.1:n.1573+5271C=
ENST00000611049.4:c.1615+5271C=	ENSP00000483084.1:n.1615+5271C=
XM_011531893.1:c.1729+5271C=	XP_011530195.1:n.1729+5271C=
XM_011531893.2:c.1942+5271C=	XP_011530195.2:n.1942+5271C=
XM_011531894.1:c.1174+5271C=	XP_011530196.1:n.1174+5271C=
XM_011531894.2:c.1174+5271C=	XP_011530196.1:n.1174+5271C=
XM_011531895.1:c.949+5271C=	XP_011530197.1:n.949+5271C=
XM_011531895.2:c.949+5271C=	XP_011530197.1:n.949+5271C=
XM_017008118.1:c.1894+5271C=	XP_016863607.1:n.1894+5271C=
XM_017008119.1:c.1726+5271C=	XP_016863608.1:n.1726+5271C=
XM_017008120.2:c.1942+5271C=	XP_016863609.1:n.1942+5271C=
XM_017008121.1:c.1942+5271C=	XP_016863610.1:n.1942+5271C=
XM_017008122.2:c.1858+5271C=	XP_016863611.1:n.1858+5271C=
XM_017008123.1:c.901+5271C=	XP_016863612.1:n.901+5271C=
XM_017008124.1:c.901+5271C=	XP_016863613.1:n.901+5271C=
XM_017008125.1:c.901+5271C=	XP_016863614.1:n.901+5271C=
XM_024454024.1:c.1906+5271C=	XP_024309792.1:n.1906+5271C=
XM_024454025.1:c.901+5271C=	XP_024309793.1:n.901+5271C=
XM_024454026.1:c.859+5271C=	XP_024309794.1:n.859+5271C=