Canonical Allele Identifier: CA2794601247

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562339_13562344del , CM000674.2:g.13562339_13562344del	GRCh38
NC_000012.11:g.13715273_13715278del , CM000674.1:g.13715273_13715278del	GRCh37
NC_000012.10:g.13606540_13606545del	NCBI36
NG_031854.1:g.422745_422750del
NG_031854.2:g.424669_424674del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*439_*444del MANE Select	ENSP00000477455.1:n.*439_*444del
ENST00000637214.1:c.69+46259_69+46264del	ENSP00000489997.1:n.69+46259_69+46264del
ENST00000609686.3:c.*439_*444del	ENSP00000477455.1:n.*439_*444del
NM_000834.3:c.*439_*444del	NP_000825.2:n.*439_*444del
XM_005253351.2:c.*439_*444del	XP_005253408.1:n.*439_*444del
XM_011520628.1:c.*439_*444del	XP_011518930.1:n.*439_*444del
XM_011520629.1:c.*439_*444del	XP_011518931.1:n.*439_*444del
XM_011520630.1:c.*439_*444del	XP_011518932.1:n.*439_*444del
NM_000834.4:c.*439_*444del	NP_000825.2:n.*439_*444del
XM_005253351.3:c.*439_*444del	XP_005253408.1:n.*439_*444del
XM_011520628.2:c.*439_*444del	XP_011518930.1:n.*439_*444del
XM_011520629.2:c.*439_*444del	XP_011518931.1:n.*439_*444del
XM_017019219.2:c.*439_*444del	XP_016874708.1:n.*439_*444del
NM_000834.5:c.*439_*444del MANE Select	NP_000825.2:n.*439_*444del