Canonical Allele Identifier: CA2017438754

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13566456_13566457delinsGA , CM000674.2:g.13566456_13566457delinsGA	GRCh38
NC_000012.11:g.13719390_13719391delinsGA , CM000674.1:g.13719390_13719391delinsGA	GRCh37
NC_000012.10:g.13610657_13610658delinsGA	NCBI36
NG_031854.1:g.418632_418633delinsTC
NG_031854.2:g.420556_420557delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2598+568_2598+569delinsTC MANE Select	ENSP00000477455.1:n.2598+568_2598+569delinsTC
ENST00000637214.1:c.69+42146_69+42147delinsTC	ENSP00000489997.1:n.69+42146_69+42147delinsTC
ENST00000609686.3:c.2598+568_2598+569delinsTC	ENSP00000477455.1:n.2598+568_2598+569delinsTC
ENST00000628166.1:n.858+568_858+569delinsTC
NM_000834.3:c.2598+568_2598+569delinsTC	NP_000825.2:n.2598+568_2598+569delinsTC
XM_005253351.2:c.384+568_384+569delinsTC	XP_005253408.1:n.384+568_384+569delinsTC
XM_011520628.1:c.2598+568_2598+569delinsTC	XP_011518930.1:n.2598+568_2598+569delinsTC
XM_011520629.1:c.2598+568_2598+569delinsTC	XP_011518931.1:n.2598+568_2598+569delinsTC
XM_011520630.1:c.2598+568_2598+569delinsTC	XP_011518932.1:n.2598+568_2598+569delinsTC
NM_000834.4:c.2598+568_2598+569delinsTC	NP_000825.2:n.2598+568_2598+569delinsTC
XM_005253351.3:c.384+568_384+569delinsTC	XP_005253408.1:n.384+568_384+569delinsTC
XM_011520628.2:c.2598+568_2598+569delinsTC	XP_011518930.1:n.2598+568_2598+569delinsTC
XM_011520629.2:c.2598+568_2598+569delinsTC	XP_011518931.1:n.2598+568_2598+569delinsTC
XM_017019219.2:c.2598+568_2598+569delinsTC	XP_016874708.1:n.2598+568_2598+569delinsTC
NM_000834.5:c.2598+568_2598+569delinsTC MANE Select	NP_000825.2:n.2598+568_2598+569delinsTC