Canonical Allele Identifier: CA2695216128

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615206_13615207dup , CM000674.2:g.13615206_13615207dup	GRCh38
NC_000012.11:g.13768140_13768141dup , CM000674.1:g.13768140_13768141dup	GRCh37
NC_000012.10:g.13659407_13659408dup	NCBI36
NG_031854.1:g.369883_369884dup
NG_031854.2:g.371807_371808dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1562_1563dup MANE Select	ENSP00000477455.1:p.Val522ArgfsTer10
ENST00000609686.3:c.1562_1563dup	ENSP00000477455.1:p.Val522ArgfsTer10
NM_000834.3:c.1562_1563dup	NP_000825.2:p.Val522ArgfsTer10
XM_011520628.1:c.1562_1563dup	XP_011518930.1:p.Val522ArgfsTer10
XM_011520629.1:c.1562_1563dup	XP_011518931.1:p.Val522ArgfsTer10
XM_011520630.1:c.1562_1563dup	XP_011518932.1:p.Val522ArgfsTer10
XR_931372.1:n.287_288dup
XR_931373.1:n.427_428dup
XR_931374.1:n.226_227dup
NM_000834.4:c.1562_1563dup	NP_000825.2:p.Val522ArgfsTer10
XM_011520628.2:c.1562_1563dup	XP_011518930.1:p.Val522ArgfsTer10
XM_011520629.2:c.1562_1563dup	XP_011518931.1:p.Val522ArgfsTer10
XM_017019219.2:c.1562_1563dup	XP_016874708.1:p.Val522ArgfsTer10
XR_001749013.1:n.708_709dup
XR_931372.2:n.424_425dup
XR_931373.2:n.566_567dup
NM_000834.5:c.1562_1563dup MANE Select	NP_000825.2:p.Val522ArgfsTer10