Canonical Allele Identifier: CA2017437743

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562568_13562571delinsGGAA , CM000674.2:g.13562568_13562571delinsGGAA	GRCh38
NC_000012.11:g.13715502_13715505delinsGGAA , CM000674.1:g.13715502_13715505delinsGGAA	GRCh37
NC_000012.10:g.13606769_13606772delinsGGAA	NCBI36
NG_031854.1:g.422518_422521delinsTTCC
NG_031854.2:g.424442_424445delinsTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*212_*215delinsTTCC MANE Select	ENSP00000477455.1:n.*212_*215delinsTTCC
ENST00000637214.1:c.69+46032_69+46035delinsTTCC	ENSP00000489997.1:n.69+46032_69+46035delinsTTCC
ENST00000609686.3:c.*212_*215delinsTTCC	ENSP00000477455.1:n.*212_*215delinsTTCC
NM_000834.3:c.*212_*215delinsTTCC	NP_000825.2:n.*212_*215delinsTTCC
XM_005253351.2:c.*212_*215delinsTTCC	XP_005253408.1:n.*212_*215delinsTTCC
XM_011520628.1:c.*212_*215delinsTTCC	XP_011518930.1:n.*212_*215delinsTTCC
XM_011520629.1:c.*212_*215delinsTTCC	XP_011518931.1:n.*212_*215delinsTTCC
XM_011520630.1:c.*212_*215delinsTTCC	XP_011518932.1:n.*212_*215delinsTTCC
NM_000834.4:c.*212_*215delinsTTCC	NP_000825.2:n.*212_*215delinsTTCC
XM_005253351.3:c.*212_*215delinsTTCC	XP_005253408.1:n.*212_*215delinsTTCC
XM_011520628.2:c.*212_*215delinsTTCC	XP_011518930.1:n.*212_*215delinsTTCC
XM_011520629.2:c.*212_*215delinsTTCC	XP_011518931.1:n.*212_*215delinsTTCC
XM_017019219.2:c.*212_*215delinsTTCC	XP_016874708.1:n.*212_*215delinsTTCC
NM_000834.5:c.*212_*215delinsTTCC MANE Select	NP_000825.2:n.*212_*215delinsTTCC