Canonical Allele Identifier: CA2017437716

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562516_13562518delinsTGA , CM000674.2:g.13562516_13562518delinsTGA	GRCh38
NC_000012.11:g.13715450_13715452delinsTGA , CM000674.1:g.13715450_13715452delinsTGA	GRCh37
NC_000012.10:g.13606717_13606719delinsTGA	NCBI36
NG_031854.1:g.422571_422573delinsTCA
NG_031854.2:g.424495_424497delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*265_*267delinsTCA MANE Select	ENSP00000477455.1:n.*265_*267delinsTCA
ENST00000637214.1:c.69+46085_69+46087delinsTCA	ENSP00000489997.1:n.69+46085_69+46087delinsTCA
ENST00000609686.3:c.*265_*267delinsTCA	ENSP00000477455.1:n.*265_*267delinsTCA
NM_000834.3:c.*265_*267delinsTCA	NP_000825.2:n.*265_*267delinsTCA
XM_005253351.2:c.*265_*267delinsTCA	XP_005253408.1:n.*265_*267delinsTCA
XM_011520628.1:c.*265_*267delinsTCA	XP_011518930.1:n.*265_*267delinsTCA
XM_011520629.1:c.*265_*267delinsTCA	XP_011518931.1:n.*265_*267delinsTCA
XM_011520630.1:c.*265_*267delinsTCA	XP_011518932.1:n.*265_*267delinsTCA
NM_000834.4:c.*265_*267delinsTCA	NP_000825.2:n.*265_*267delinsTCA
XM_005253351.3:c.*265_*267delinsTCA	XP_005253408.1:n.*265_*267delinsTCA
XM_011520628.2:c.*265_*267delinsTCA	XP_011518930.1:n.*265_*267delinsTCA
XM_011520629.2:c.*265_*267delinsTCA	XP_011518931.1:n.*265_*267delinsTCA
XM_017019219.2:c.*265_*267delinsTCA	XP_016874708.1:n.*265_*267delinsTCA
NM_000834.5:c.*265_*267delinsTCA MANE Select	NP_000825.2:n.*265_*267delinsTCA