Canonical Allele Identifier: CA2017437611

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562290_13562291delinsAG , CM000674.2:g.13562290_13562291delinsAG	GRCh38
NC_000012.11:g.13715224_13715225delinsAG , CM000674.1:g.13715224_13715225delinsAG	GRCh37
NC_000012.10:g.13606491_13606492delinsAG	NCBI36
NG_031854.1:g.422798_422799delinsCT
NG_031854.2:g.424722_424723delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*492_*493delinsCT MANE Select	ENSP00000477455.1:n.*492_*493delinsCT
ENST00000636207.1:n.1_2delinsCT
ENST00000637214.1:c.69+46312_69+46313delinsCT	ENSP00000489997.1:n.69+46312_69+46313delinsCT
ENST00000609686.3:c.*492_*493delinsCT	ENSP00000477455.1:n.*492_*493delinsCT
NM_000834.3:c.*492_*493delinsCT	NP_000825.2:n.*492_*493delinsCT
XM_005253351.2:c.*492_*493delinsCT	XP_005253408.1:n.*492_*493delinsCT
XM_011520628.1:c.*492_*493delinsCT	XP_011518930.1:n.*492_*493delinsCT
XM_011520629.1:c.*492_*493delinsCT	XP_011518931.1:n.*492_*493delinsCT
XM_011520630.1:c.*492_*493delinsCT	XP_011518932.1:n.*492_*493delinsCT
NM_000834.4:c.*492_*493delinsCT	NP_000825.2:n.*492_*493delinsCT
XM_005253351.3:c.*492_*493delinsCT	XP_005253408.1:n.*492_*493delinsCT
XM_011520628.2:c.*492_*493delinsCT	XP_011518930.1:n.*492_*493delinsCT
XM_011520629.2:c.*492_*493delinsCT	XP_011518931.1:n.*492_*493delinsCT
XM_017019219.2:c.*492_*493delinsCT	XP_016874708.1:n.*492_*493delinsCT
NM_000834.5:c.*492_*493delinsCT MANE Select	NP_000825.2:n.*492_*493delinsCT