Canonical Allele Identifier: CA2617757454

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13754031-A-AAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13754032_13754033insGTA , CM000674.2:g.13754032_13754033insGTA	GRCh38
NC_000012.11:g.13906966_13906967insGTA , CM000674.1:g.13906966_13906967insGTA	GRCh37
NC_000012.10:g.13798233_13798234insGTA	NCBI36
NG_031854.1:g.231057_231058insACT
NG_031854.2:g.232981_232982insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.412-117_412-116insACT MANE Select	ENSP00000477455.1:n.412-117_412-116insACT
ENST00000630791.2:c.412-117_412-116insACT	ENSP00000486677.2:n.412-117_412-116insACT
ENST00000609686.3:c.412-117_412-116insACT	ENSP00000477455.1:n.412-117_412-116insACT
NM_000834.3:c.412-117_412-116insACT	NP_000825.2:n.412-117_412-116insACT
XM_011520628.1:c.412-117_412-116insACT	XP_011518930.1:n.412-117_412-116insACT
XM_011520629.1:c.412-117_412-116insACT	XP_011518931.1:n.412-117_412-116insACT
XM_011520630.1:c.412-117_412-116insACT	XP_011518932.1:n.412-117_412-116insACT
NM_000834.4:c.412-117_412-116insACT	NP_000825.2:n.412-117_412-116insACT
XM_011520628.2:c.412-117_412-116insACT	XP_011518930.1:n.412-117_412-116insACT
XM_011520629.2:c.412-117_412-116insACT	XP_011518931.1:n.412-117_412-116insACT
XM_017019219.2:c.412-117_412-116insACT	XP_016874708.1:n.412-117_412-116insACT
NM_000834.5:c.412-117_412-116insACT MANE Select	NP_000825.2:n.412-117_412-116insACT