Canonical Allele Identifier: CA1476836318

Gene: GRID2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775948_92775950delinsAAT , CM000666.2:g.92775948_92775950delinsAAT	GRCh38
NC_000004.11:g.93697099_93697101delinsAAT , CM000666.1:g.93697099_93697101delinsAAT	GRCh37
NC_000004.10:g.93916122_93916124delinsAAT	NCBI36
NG_034113.1:g.476550_476552delinsAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185662_244+185664delinsAAT MANE Select	ENSP00000282020.4:n.244+185662_244+185664...
ENST00000282020.8:c.244+185662_244+185664delinsAAT	ENSP00000282020.4:n.244+185662_244+185664...
ENST00000505687.5:n.416+185662_416+185664delinsAAT
ENST00000510992.5:c.244+185662_244+185664delinsAAT	ENSP00000421257.1:n.244+185662_244+185664...
NM_001286838.1:c.244+185662_244+185664delinsAAT	NP_001273767.1:n.244+185662_244+185664del...
NM_001510.3:c.244+185662_244+185664delinsAAT	NP_001501.2:n.244+185662_244+185664delins...
XM_017008122.2:c.244+185662_244+185664delinsAAT	XP_016863611.1:n.244+185662_244+185664del...
XM_024454024.1:c.244+185662_244+185664delinsAAT	XP_024309792.1:n.244+185662_244+185664del...
NM_001510.4:c.244+185662_244+185664delinsAAT MANE Select	NP_001501.2:n.244+185662_244+185664delins...