Canonical Allele Identifier: CA2017525866

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753522_13753524delinsCTG , CM000674.2:g.13753522_13753524delinsCTG	GRCh38
NC_000012.11:g.13906456_13906458delinsCTG , CM000674.1:g.13906456_13906458delinsCTG	GRCh37
NC_000012.10:g.13797723_13797725delinsCTG	NCBI36
NG_031854.1:g.231565_231567delinsCAG
NG_031854.2:g.233489_233491delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.803_805delinsCAG MANE Select	ENSP00000477455.1:p.Thr268=
ENST00000630791.2:c.803_805delinsCAG	ENSP00000486677.2:p.Thr268=
ENST00000609686.3:c.803_805delinsCAG	ENSP00000477455.1:p.Thr268=
NM_000834.3:c.803_805delinsCAG	NP_000825.2:p.Thr268=
XM_011520628.1:c.803_805delinsCAG	XP_011518930.1:p.Thr268=
XM_011520629.1:c.803_805delinsCAG	XP_011518931.1:p.Thr268=
XM_011520630.1:c.803_805delinsCAG	XP_011518932.1:p.Thr268=
NM_000834.4:c.803_805delinsCAG	NP_000825.2:p.Thr268=
XM_011520628.2:c.803_805delinsCAG	XP_011518930.1:p.Thr268=
XM_011520629.2:c.803_805delinsCAG	XP_011518931.1:p.Thr268=
XM_017019219.2:c.803_805delinsCAG	XP_016874708.1:p.Thr268=
NM_000834.5:c.803_805delinsCAG MANE Select	NP_000825.2:p.Thr268=