Canonical Allele Identifier: CA2017437551

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562178_13562179delinsTC , CM000674.2:g.13562178_13562179delinsTC	GRCh38
NC_000012.11:g.13715112_13715113delinsTC , CM000674.1:g.13715112_13715113delinsTC	GRCh37
NC_000012.10:g.13606379_13606380delinsTC	NCBI36
NG_031854.1:g.422910_422911delinsGA
NG_031854.2:g.424834_424835delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*604_*605delinsGA MANE Select	ENSP00000477455.1:n.*604_*605delinsGA
ENST00000636207.1:n.54+59_54+60delinsGA
ENST00000637214.1:c.69+46424_69+46425delinsGA	ENSP00000489997.1:n.69+46424_69+46425delinsGA
ENST00000609686.3:c.*604_*605delinsGA	ENSP00000477455.1:n.*604_*605delinsGA
NM_000834.3:c.*604_*605delinsGA	NP_000825.2:n.*604_*605delinsGA
XM_005253351.2:c.*604_*605delinsGA	XP_005253408.1:n.*604_*605delinsGA
XM_011520628.1:c.*604_*605delinsGA	XP_011518930.1:n.*604_*605delinsGA
XM_011520629.1:c.*604_*605delinsGA	XP_011518931.1:n.*604_*605delinsGA
XM_011520630.1:c.*604_*605delinsGA	XP_011518932.1:n.*604_*605delinsGA
NM_000834.4:c.*604_*605delinsGA	NP_000825.2:n.*604_*605delinsGA
XM_005253351.3:c.*604_*605delinsGA	XP_005253408.1:n.*604_*605delinsGA
XM_011520628.2:c.*604_*605delinsGA	XP_011518930.1:n.*604_*605delinsGA
XM_011520629.2:c.*604_*605delinsGA	XP_011518931.1:n.*604_*605delinsGA
XM_017019219.2:c.*604_*605delinsGA	XP_016874708.1:n.*604_*605delinsGA
NM_000834.5:c.*604_*605delinsGA MANE Select	NP_000825.2:n.*604_*605delinsGA