Canonical Allele Identifier: CA2017437761

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562595_13562597delinsGGA , CM000674.2:g.13562595_13562597delinsGGA	GRCh38
NC_000012.11:g.13715529_13715531delinsGGA , CM000674.1:g.13715529_13715531delinsGGA	GRCh37
NC_000012.10:g.13606796_13606798delinsGGA	NCBI36
NG_031854.1:g.422492_422494delinsTCC
NG_031854.2:g.424416_424418delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*186_*188delinsTCC MANE Select	ENSP00000477455.1:n.*186_*188delinsTCC
ENST00000637214.1:c.69+46006_69+46008delinsTCC	ENSP00000489997.1:n.69+46006_69+46008delinsTCC
ENST00000609686.3:c.*186_*188delinsTCC	ENSP00000477455.1:n.*186_*188delinsTCC
NM_000834.3:c.*186_*188delinsTCC	NP_000825.2:n.*186_*188delinsTCC
XM_005253351.2:c.*186_*188delinsTCC	XP_005253408.1:n.*186_*188delinsTCC
XM_011520628.1:c.*186_*188delinsTCC	XP_011518930.1:n.*186_*188delinsTCC
XM_011520629.1:c.*186_*188delinsTCC	XP_011518931.1:n.*186_*188delinsTCC
XM_011520630.1:c.*186_*188delinsTCC	XP_011518932.1:n.*186_*188delinsTCC
NM_000834.4:c.*186_*188delinsTCC	NP_000825.2:n.*186_*188delinsTCC
XM_005253351.3:c.*186_*188delinsTCC	XP_005253408.1:n.*186_*188delinsTCC
XM_011520628.2:c.*186_*188delinsTCC	XP_011518930.1:n.*186_*188delinsTCC
XM_011520629.2:c.*186_*188delinsTCC	XP_011518931.1:n.*186_*188delinsTCC
XM_017019219.2:c.*186_*188delinsTCC	XP_016874708.1:n.*186_*188delinsTCC
NM_000834.5:c.*186_*188delinsTCC MANE Select	NP_000825.2:n.*186_*188delinsTCC