Canonical Allele Identifier: CA2559939796

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753948_13753949insTAG , CM000674.2:g.13753948_13753949insTAG	GRCh38
NC_000012.11:g.13906882_13906883insTAG , CM000674.1:g.13906882_13906883insTAG	GRCh37
NC_000012.10:g.13798149_13798150insTAG	NCBI36
NG_031854.1:g.231140_231141insCTA
NG_031854.2:g.233064_233065insCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.412-34_412-33insCTA MANE Select	ENSP00000477455.1:n.412-34_412-33insCTA
ENST00000630791.2:c.412-34_412-33insCTA	ENSP00000486677.2:n.412-34_412-33insCTA
ENST00000609686.3:c.412-34_412-33insCTA	ENSP00000477455.1:n.412-34_412-33insCTA
NM_000834.3:c.412-34_412-33insCTA	NP_000825.2:n.412-34_412-33insCTA
XM_011520628.1:c.412-34_412-33insCTA	XP_011518930.1:n.412-34_412-33insCTA
XM_011520629.1:c.412-34_412-33insCTA	XP_011518931.1:n.412-34_412-33insCTA
XM_011520630.1:c.412-34_412-33insCTA	XP_011518932.1:n.412-34_412-33insCTA
NM_000834.4:c.412-34_412-33insCTA	NP_000825.2:n.412-34_412-33insCTA
XM_011520628.2:c.412-34_412-33insCTA	XP_011518930.1:n.412-34_412-33insCTA
XM_011520629.2:c.412-34_412-33insCTA	XP_011518931.1:n.412-34_412-33insCTA
XM_017019219.2:c.412-34_412-33insCTA	XP_016874708.1:n.412-34_412-33insCTA
NM_000834.5:c.412-34_412-33insCTA MANE Select	NP_000825.2:n.412-34_412-33insCTA