Canonical Allele Identifier: CA1476836323

Gene: GRID2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775958_92775961delinsTCTG , CM000666.2:g.92775958_92775961delinsTCTG	GRCh38
NC_000004.11:g.93697109_93697112delinsTCTG , CM000666.1:g.93697109_93697112delinsTCTG	GRCh37
NC_000004.10:g.93916132_93916135delinsTCTG	NCBI36
NG_034113.1:g.476560_476563delinsTCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185672_244+185675delinsTCTG MANE Select	ENSP00000282020.4:n.244+185672_244+185675...
ENST00000282020.8:c.244+185672_244+185675delinsTCTG	ENSP00000282020.4:n.244+185672_244+185675...
ENST00000505687.5:n.416+185672_416+185675delinsTCTG
ENST00000510992.5:c.244+185672_244+185675delinsTCTG	ENSP00000421257.1:n.244+185672_244+185675...
NM_001286838.1:c.244+185672_244+185675delinsTCTG	NP_001273767.1:n.244+185672_244+185675del...
NM_001510.3:c.244+185672_244+185675delinsTCTG	NP_001501.2:n.244+185672_244+185675delins...
XM_017008122.2:c.244+185672_244+185675delinsTCTG	XP_016863611.1:n.244+185672_244+185675del...
XM_024454024.1:c.244+185672_244+185675delinsTCTG	XP_024309792.1:n.244+185672_244+185675del...
NM_001510.4:c.244+185672_244+185675delinsTCTG MANE Select	NP_001501.2:n.244+185672_244+185675delins...