Canonical Allele Identifier: CA2017437059

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561283_13561285delinsCTG , CM000674.2:g.13561283_13561285delinsCTG	GRCh38
NC_000012.11:g.13714217_13714219delinsCTG , CM000674.1:g.13714217_13714219delinsCTG	GRCh37
NC_000012.10:g.13605484_13605486delinsCTG	NCBI36
NG_031854.1:g.423804_423806delinsCAG
NG_031854.2:g.425728_425730delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*1498_*1500delinsCAG MANE Select	ENSP00000477455.1:n.*1498_*1500delinsCAG
ENST00000637214.1:c.69+47318_69+47320delinsCAG	ENSP00000489997.1:n.69+47318_69+47320delinsCAG
ENST00000609686.3:c.*1498_*1500delinsCAG	ENSP00000477455.1:n.*1498_*1500delinsCAG
XM_005253351.2:c.*1498_*1500delinsCAG	XP_005253408.1:n.*1498_*1500delinsCAG
XM_011520628.1:c.*1498_*1500delinsCAG	XP_011518930.1:n.*1498_*1500delinsCAG
XM_011520629.1:c.*1498_*1500delinsCAG	XP_011518931.1:n.*1498_*1500delinsCAG
XM_011520630.1:c.*1498_*1500delinsCAG	XP_011518932.1:n.*1498_*1500delinsCAG
NM_000834.4:c.*1498_*1500delinsCAG	NP_000825.2:n.*1498_*1500delinsCAG
XM_005253351.3:c.*1498_*1500delinsCAG	XP_005253408.1:n.*1498_*1500delinsCAG
XM_011520628.2:c.*1498_*1500delinsCAG	XP_011518930.1:n.*1498_*1500delinsCAG
XM_011520629.2:c.*1498_*1500delinsCAG	XP_011518931.1:n.*1498_*1500delinsCAG
XM_017019219.2:c.*1498_*1500delinsCAG	XP_016874708.1:n.*1498_*1500delinsCAG
NM_000834.5:c.*1498_*1500delinsCAG MANE Select	NP_000825.2:n.*1498_*1500delinsCAG