Canonical Allele Identifier: CA2017437648

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562378_13562379delinsTG , CM000674.2:g.13562378_13562379delinsTG	GRCh38
NC_000012.11:g.13715312_13715313delinsTG , CM000674.1:g.13715312_13715313delinsTG	GRCh37
NC_000012.10:g.13606579_13606580delinsTG	NCBI36
NG_031854.1:g.422710_422711delinsCA
NG_031854.2:g.424634_424635delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*404_*405delinsCA MANE Select	ENSP00000477455.1:n.*404_*405delinsCA
ENST00000637214.1:c.69+46224_69+46225delinsCA	ENSP00000489997.1:n.69+46224_69+46225delinsCA
ENST00000609686.3:c.*404_*405delinsCA	ENSP00000477455.1:n.*404_*405delinsCA
NM_000834.3:c.*404_*405delinsCA	NP_000825.2:n.*404_*405delinsCA
XM_005253351.2:c.*404_*405delinsCA	XP_005253408.1:n.*404_*405delinsCA
XM_011520628.1:c.*404_*405delinsCA	XP_011518930.1:n.*404_*405delinsCA
XM_011520629.1:c.*404_*405delinsCA	XP_011518931.1:n.*404_*405delinsCA
XM_011520630.1:c.*404_*405delinsCA	XP_011518932.1:n.*404_*405delinsCA
NM_000834.4:c.*404_*405delinsCA	NP_000825.2:n.*404_*405delinsCA
XM_005253351.3:c.*404_*405delinsCA	XP_005253408.1:n.*404_*405delinsCA
XM_011520628.2:c.*404_*405delinsCA	XP_011518930.1:n.*404_*405delinsCA
XM_011520629.2:c.*404_*405delinsCA	XP_011518931.1:n.*404_*405delinsCA
XM_017019219.2:c.*404_*405delinsCA	XP_016874708.1:n.*404_*405delinsCA
NM_000834.5:c.*404_*405delinsCA MANE Select	NP_000825.2:n.*404_*405delinsCA