Canonical Allele Identifier: CA2017463499

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615684_13615688delinsAAAAC , CM000674.2:g.13615684_13615688delinsAAAAC	GRCh38
NC_000012.11:g.13768618_13768622delinsAAAAC , CM000674.1:g.13768618_13768622delinsAAAAC	GRCh37
NC_000012.10:g.13659885_13659889delinsAAAAC	NCBI36
NG_031854.1:g.369401_369405delinsGTTTT
NG_031854.2:g.371325_371329delinsGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-24_1329-20delinsGTTTT MANE Select	ENSP00000477455.1:n.1329-24_1329-20delinsGTTTT
ENST00000630791.2:c.1329-24_1329-20delinsGTTTT	ENSP00000486677.2:n.1329-24_1329-20delinsGTTTT
ENST00000609686.3:c.1329-24_1329-20delinsGTTTT	ENSP00000477455.1:n.1329-24_1329-20delinsGTTTT
NM_000834.3:c.1329-24_1329-20delinsGTTTT	NP_000825.2:n.1329-24_1329-20delinsGTTTT
XM_011520628.1:c.1329-24_1329-20delinsGTTTT	XP_011518930.1:n.1329-24_1329-20delinsGTTTT
XM_011520629.1:c.1329-24_1329-20delinsGTTTT	XP_011518931.1:n.1329-24_1329-20delinsGTTTT
XM_011520630.1:c.1329-24_1329-20delinsGTTTT	XP_011518932.1:n.1329-24_1329-20delinsGTTTT
XR_931372.1:n.307+458_307+462delinsAAAAC
XR_931373.1:n.447+458_447+462delinsAAAAC
XR_931374.1:n.246+458_246+462delinsAAAAC
NM_000834.4:c.1329-24_1329-20delinsGTTTT	NP_000825.2:n.1329-24_1329-20delinsGTTTT
XM_011520628.2:c.1329-24_1329-20delinsGTTTT	XP_011518930.1:n.1329-24_1329-20delinsGTTTT
XM_011520629.2:c.1329-24_1329-20delinsGTTTT	XP_011518931.1:n.1329-24_1329-20delinsGTTTT
XM_017019219.2:c.1329-24_1329-20delinsGTTTT	XP_016874708.1:n.1329-24_1329-20delinsGTTTT
XR_001749013.1:n.728+458_728+462delinsAAAAC
XR_931372.2:n.444+458_444+462delinsAAAAC
XR_931373.2:n.586+458_586+462delinsAAAAC
NM_000834.5:c.1329-24_1329-20delinsGTTTT MANE Select	NP_000825.2:n.1329-24_1329-20delinsGTTTT