Canonical Allele Identifier: CA1476836345

Gene: GRID2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92776002C= , CM000666.2:g.92776002C=	GRCh38
NC_000004.11:g.93697153C= , CM000666.1:g.93697153C=	GRCh37
NC_000004.10:g.93916176C=	NCBI36
NG_034113.1:g.476604C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001510.4:c.244+185716C= MANE Select	NP_001501.2:n.244+185716C=
ENST00000282020.9:c.244+185716C= MANE Select	ENSP00000282020.4:n.244+185716C=
NM_001286838.1:c.244+185716C=	NP_001273767.1:n.244+185716C=
NM_001510.3:c.244+185716C=	NP_001501.2:n.244+185716C=
ENST00000282020.8:c.244+185716C=	ENSP00000282020.4:n.244+185716C=
ENST00000505687.5:n.416+185716C=
ENST00000510992.5:c.244+185716C=	ENSP00000421257.1:n.244+185716C=
XM_017008122.2:c.244+185716C=	XP_016863611.1:n.244+185716C=
XM_024454024.1:c.244+185716C=	XP_024309792.1:n.244+185716C=