Canonical Allele Identifier: CA1476836385

Gene: GRID2

Linked Data

• dbSNP Id: rs1738777404

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92776052_92776053del , CM000666.2:g.92776052_92776053del	GRCh38
NC_000004.11:g.93697203_93697204del , CM000666.1:g.93697203_93697204del	GRCh37
NC_000004.10:g.93916226_93916227del	NCBI36
NG_034113.1:g.476654_476655del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282020.9:c.244+185766_244+185767del MANE Select	ENSP00000282020.4:n.244+185766_244+185767del
ENST00000282020.8:c.244+185766_244+185767del	ENSP00000282020.4:n.244+185766_244+185767del
ENST00000505687.5:n.416+185766_416+185767del
ENST00000510992.5:c.244+185766_244+185767del	ENSP00000421257.1:n.244+185766_244+185767del
NM_001286838.1:c.244+185766_244+185767del	NP_001273767.1:n.244+185766_244+185767del
NM_001510.3:c.244+185766_244+185767del	NP_001501.2:n.244+185766_244+185767del
XM_017008122.2:c.244+185766_244+185767del	XP_016863611.1:n.244+185766_244+185767del
XM_024454024.1:c.244+185766_244+185767del	XP_024309792.1:n.244+185766_244+185767del
NM_001510.4:c.244+185766_244+185767del MANE Select	NP_001501.2:n.244+185766_244+185767del