Canonical Allele Identifier: CA645585653

Gene: GRIN2B

Linked Data

• COSMIC: COSM5007927

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615626_13615627insT , CM000674.2:g.13615626_13615627insT	GRCh38
NC_000012.11:g.13768560_13768561insT , CM000674.1:g.13768560_13768561insT	GRCh37
NC_000012.10:g.13659827_13659828insT	NCBI36
NG_031854.1:g.369462_369463insA
NG_031854.2:g.371386_371387insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1366_1367insA MANE Select	ENSP00000477455.1:p.Cys456Ter
ENST00000630791.2:c.1366_1367insA	ENSP00000486677.2:p.Cys456Ter
ENST00000609686.3:c.1366_1367insA	ENSP00000477455.1:p.Cys456Ter
NM_000834.3:c.1366_1367insA	NP_000825.2:p.Cys456Ter
XM_011520628.1:c.1366_1367insA	XP_011518930.1:p.Cys456Ter
XM_011520629.1:c.1366_1367insA	XP_011518931.1:p.Cys456Ter
XM_011520630.1:c.1366_1367insA	XP_011518932.1:p.Cys456Ter
XR_931372.1:n.307+400_307+401insT
XR_931373.1:n.447+400_447+401insT
XR_931374.1:n.246+400_246+401insT
NM_000834.4:c.1366_1367insA	NP_000825.2:p.Cys456Ter
XM_011520628.2:c.1366_1367insA	XP_011518930.1:p.Cys456Ter
XM_011520629.2:c.1366_1367insA	XP_011518931.1:p.Cys456Ter
XM_017019219.2:c.1366_1367insA	XP_016874708.1:p.Cys456Ter
XR_001749013.1:n.728+400_728+401insT
XR_931372.2:n.444+400_444+401insT
XR_931373.2:n.586+400_586+401insT
NM_000834.5:c.1366_1367insA MANE Select	NP_000825.2:p.Cys456Ter