Canonical Allele Identifier: CA2017437554

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562183_13562184delinsTG , CM000674.2:g.13562183_13562184delinsTG	GRCh38
NC_000012.11:g.13715117_13715118delinsTG , CM000674.1:g.13715117_13715118delinsTG	GRCh37
NC_000012.10:g.13606384_13606385delinsTG	NCBI36
NG_031854.1:g.422905_422906delinsCA
NG_031854.2:g.424829_424830delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*599_*600delinsCA MANE Select	ENSP00000477455.1:n.*599_*600delinsCA
ENST00000636207.1:n.54+54_54+55delinsCA
ENST00000637214.1:c.69+46419_69+46420delinsCA	ENSP00000489997.1:n.69+46419_69+46420delinsCA
ENST00000609686.3:c.*599_*600delinsCA	ENSP00000477455.1:n.*599_*600delinsCA
NM_000834.3:c.*599_*600delinsCA	NP_000825.2:n.*599_*600delinsCA
XM_005253351.2:c.*599_*600delinsCA	XP_005253408.1:n.*599_*600delinsCA
XM_011520628.1:c.*599_*600delinsCA	XP_011518930.1:n.*599_*600delinsCA
XM_011520629.1:c.*599_*600delinsCA	XP_011518931.1:n.*599_*600delinsCA
XM_011520630.1:c.*599_*600delinsCA	XP_011518932.1:n.*599_*600delinsCA
NM_000834.4:c.*599_*600delinsCA	NP_000825.2:n.*599_*600delinsCA
XM_005253351.3:c.*599_*600delinsCA	XP_005253408.1:n.*599_*600delinsCA
XM_011520628.2:c.*599_*600delinsCA	XP_011518930.1:n.*599_*600delinsCA
XM_011520629.2:c.*599_*600delinsCA	XP_011518931.1:n.*599_*600delinsCA
XM_017019219.2:c.*599_*600delinsCA	XP_016874708.1:n.*599_*600delinsCA
NM_000834.5:c.*599_*600delinsCA MANE Select	NP_000825.2:n.*599_*600delinsCA