Canonical Allele Identifier: CA1476836304

Gene: GRID2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775918A= , CM000666.2:g.92775918A=	GRCh38
NC_000004.11:g.93697069A= , CM000666.1:g.93697069A=	GRCh37
NC_000004.10:g.93916092A=	NCBI36
NG_034113.1:g.476520A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185632A= MANE Select	ENSP00000282020.4:n.244+185632A=
ENST00000282020.8:c.244+185632A=	ENSP00000282020.4:n.244+185632A=
ENST00000505687.5:n.416+185632A=
ENST00000510992.5:c.244+185632A=	ENSP00000421257.1:n.244+185632A=
NM_001286838.1:c.244+185632A=	NP_001273767.1:n.244+185632A=
NM_001510.3:c.244+185632A=	NP_001501.2:n.244+185632A=
XM_017008122.2:c.244+185632A=	XP_016863611.1:n.244+185632A=
XM_024454024.1:c.244+185632A=	XP_024309792.1:n.244+185632A=
NM_001510.4:c.244+185632A= MANE Select	NP_001501.2:n.244+185632A=