Canonical Allele Identifier: CA2617717792

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13561357-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561360del , CM000674.2:g.13561360del	GRCh38
NC_000012.11:g.13714294del , CM000674.1:g.13714294del	GRCh37
NC_000012.10:g.13605561del	NCBI36
NG_031854.1:g.423731del
NG_031854.2:g.425655del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1425del MANE Select	ENSP00000477455.1:n.*1425del
ENST00000637214.1:c.69+47245del	ENSP00000489997.1:n.69+47245del
ENST00000609686.3:c.*1425del	ENSP00000477455.1:n.*1425del
XM_005253351.2:c.*1425del	XP_005253408.1:n.*1425del
XM_011520628.1:c.*1425del	XP_011518930.1:n.*1425del
XM_011520629.1:c.*1425del	XP_011518931.1:n.*1425del
XM_011520630.1:c.*1425del	XP_011518932.1:n.*1425del
NM_000834.4:c.*1425del	NP_000825.2:n.*1425del
XM_005253351.3:c.*1425del	XP_005253408.1:n.*1425del
XM_011520628.2:c.*1425del	XP_011518930.1:n.*1425del
XM_011520629.2:c.*1425del	XP_011518931.1:n.*1425del
XM_017019219.2:c.*1425del	XP_016874708.1:n.*1425del
NM_000834.5:c.*1425del MANE Select	NP_000825.2:n.*1425del