Canonical Allele Identifier: CA2017437574

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562223_13562234delinsAAATGGCCTCCC , CM000674.2:g.13562223_13562234delinsAAATGGCCTCCC	GRCh38
NC_000012.11:g.13715157_13715168delinsAAATGGCCTCCC , CM000674.1:g.13715157_13715168delinsAAATGGCCTCCC	GRCh37
NC_000012.10:g.13606424_13606435delinsAAATGGCCTCCC	NCBI36
NG_031854.1:g.422855_422866delinsGGGAGGCCATTT
NG_031854.2:g.424779_424790delinsGGGAGGCCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*549_*560delinsGGGAGGCCATTT MANE Select	ENSP00000477455.1:n.*549_*560delinsGGGAGGCCATTT
ENST00000636207.1:n.54+4_54+15delinsGGGAGGCCATTT
ENST00000637214.1:c.69+46369_69+46380delinsGGGAGGCCATTT	ENSP00000489997.1:n.69+46369_69+46380delinsGGGAGGCCATTT
ENST00000609686.3:c.*549_*560delinsGGGAGGCCATTT	ENSP00000477455.1:n.*549_*560delinsGGGAGGCCATTT
NM_000834.3:c.*549_*560delinsGGGAGGCCATTT	NP_000825.2:n.*549_*560delinsGGGAGGCCATTT
XM_005253351.2:c.*549_*560delinsGGGAGGCCATTT	XP_005253408.1:n.*549_*560delinsGGGAGGCCATTT
XM_011520628.1:c.*549_*560delinsGGGAGGCCATTT	XP_011518930.1:n.*549_*560delinsGGGAGGCCATTT
XM_011520629.1:c.*549_*560delinsGGGAGGCCATTT	XP_011518931.1:n.*549_*560delinsGGGAGGCCATTT
XM_011520630.1:c.*549_*560delinsGGGAGGCCATTT	XP_011518932.1:n.*549_*560delinsGGGAGGCCATTT
NM_000834.4:c.*549_*560delinsGGGAGGCCATTT	NP_000825.2:n.*549_*560delinsGGGAGGCCATTT
XM_005253351.3:c.*549_*560delinsGGGAGGCCATTT	XP_005253408.1:n.*549_*560delinsGGGAGGCCATTT
XM_011520628.2:c.*549_*560delinsGGGAGGCCATTT	XP_011518930.1:n.*549_*560delinsGGGAGGCCATTT
XM_011520629.2:c.*549_*560delinsGGGAGGCCATTT	XP_011518931.1:n.*549_*560delinsGGGAGGCCATTT
XM_017019219.2:c.*549_*560delinsGGGAGGCCATTT	XP_016874708.1:n.*549_*560delinsGGGAGGCCATTT
NM_000834.5:c.*549_*560delinsGGGAGGCCATTT MANE Select	NP_000825.2:n.*549_*560delinsGGGAGGCCATTT