Canonical Allele Identifier: CA2794601901

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608949_13608950insACACACCCAACACA , CM000674.2:g.13608949_13608950insACACACCCAACACA	GRCh38
NC_000012.11:g.13761883_13761884insACACACCCAACACA , CM000674.1:g.13761883_13761884insACACACCCAACACA	GRCh37
NC_000012.10:g.13653150_13653151insACACACCCAACACA	NCBI36
NG_031854.1:g.376140_376141insGTGTTGGGTGTGTT
NG_031854.2:g.378064_378065insGTGTTGGGTGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-117_1781-116insGTGTTGGGTGTGTT MANE Select	ENSP00000477455.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
ENST00000628166.2:n.41-117_41-116insGTGTTGGGTGTGTT
ENST00000609686.3:c.1781-117_1781-116insGTGTTGGGTGTGTT	ENSP00000477455.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
ENST00000628166.1:n.41-117_41-116insGTGTTGGGTGTGTT
NM_000834.3:c.1781-117_1781-116insGTGTTGGGTGTGTT	NP_000825.2:n.1781-117_1781-116insGTGTTGGGTGTGTT
XM_011520628.1:c.1781-117_1781-116insGTGTTGGGTGTGTT	XP_011518930.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
XM_011520629.1:c.1781-117_1781-116insGTGTTGGGTGTGTT	XP_011518931.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
XM_011520630.1:c.1781-117_1781-116insGTGTTGGGTGTGTT	XP_011518932.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
XR_931372.1:n.179-6149_179-6148insACACACCCAACACA
XR_931373.1:n.318+192_318+193insACACACCCAACACA
NM_000834.4:c.1781-117_1781-116insGTGTTGGGTGTGTT	NP_000825.2:n.1781-117_1781-116insGTGTTGGGTGTGTT
XM_011520628.2:c.1781-117_1781-116insGTGTTGGGTGTGTT	XP_011518930.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
XM_011520629.2:c.1781-117_1781-116insGTGTTGGGTGTGTT	XP_011518931.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
XM_017019219.2:c.1781-117_1781-116insGTGTTGGGTGTGTT	XP_016874708.1:n.1781-117_1781-116insGTGTTGGGTGTGTT
XR_001749013.1:n.457+192_457+193insACACACCCAACACA
XR_931372.2:n.316-6149_316-6148insACACACCCAACACA
XR_931373.2:n.457+192_457+193insACACACCCAACACA
NM_000834.5:c.1781-117_1781-116insGTGTTGGGTGTGTT MANE Select	NP_000825.2:n.1781-117_1781-116insGTGTTGGGTGTGTT