Canonical Allele Identifier: CA2366529438

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46119319_46119320delinsTG , CM000682.2:g.46119319_46119320delinsTG	GRCh38
NC_000020.10:g.44747958_44747959delinsTG , CM000682.1:g.44747958_44747959delinsTG	GRCh37
NC_000020.9:g.44181365_44181366delinsTG	NCBI36
NG_007279.1:g.6053_6054delinsTG , LRG_40:g.6053_6054delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.51+925_51+926delinsTG	ENSP00000512095.1:n.51+925_51+926delinsTG
ENST00000489304.6:c.51+925_51+926delinsTG	ENSP00000512096.1:n.51+925_51+926delinsTG
ENST00000695669.1:n.124+925_124+926delinsTG
ENST00000695670.1:n.110+925_110+926delinsTG
ENST00000695671.1:c.51+925_51+926delinsTG	ENSP00000512093.1:n.51+925_51+926delinsTG
ENST00000695672.1:n.55+925_55+926delinsTG
ENST00000372285.8:c.51+925_51+926delinsTG MANE Select	ENSP00000361359.3:n.51+925_51+926delinsTG
ENST00000372276.7:c.51+925_51+926delinsTG	ENSP00000361350.3:n.51+925_51+926delinsTG
ENST00000372285.7:c.51+925_51+926delinsTG	ENSP00000361359.3:n.51+925_51+926delinsTG
ENST00000466205.5:c.47+925_47+926delinsTG
ENST00000477696.5:n.22+925_22+926delinsTG
ENST00000489304.5:n.44+925_44+926delinsTG
ENST00000620709.4:c.51+925_51+926delinsTG	ENSP00000484074.1:n.51+925_51+926delinsTG
NM_001250.5:c.51+925_51+926delinsTG	NP_001241.1:n.51+925_51+926delinsTG
NM_001302753.1:c.51+925_51+926delinsTG	NP_001289682.1:n.51+925_51+926delinsTG
NM_152854.3:c.51+925_51+926delinsTG	NP_690593.1:n.51+925_51+926delinsTG
NR_126502.1:n.141+925_141+926delinsTG
XM_005260617.2:c.51+925_51+926delinsTG	XP_005260674.1:n.51+925_51+926delinsTG
XM_005260619.2:c.51+925_51+926delinsTG	XP_005260676.1:n.51+925_51+926delinsTG
XM_011529109.1:c.51+925_51+926delinsTG	XP_011527411.1:n.51+925_51+926delinsTG
XR_936660.1:n.145+925_145+926delinsTG
NM_001322421.1:c.51+925_51+926delinsTG	NP_001309350.1:n.51+925_51+926delinsTG
NM_001322422.1:c.51+925_51+926delinsTG	NP_001309351.1:n.51+925_51+926delinsTG
NM_001362758.1:c.51+925_51+926delinsTG	NP_001349687.1:n.51+925_51+926delinsTG
NR_136327.1:n.141+925_141+926delinsTG
XM_005260619.3:c.51+925_51+926delinsTG	XP_005260676.1:n.51+925_51+926delinsTG
XM_011529109.2:c.51+925_51+926delinsTG	XP_011527411.1:n.51+925_51+926delinsTG
XM_017028135.1:c.51+925_51+926delinsTG	XP_016883624.1:n.51+925_51+926delinsTG
XM_017028136.1:c.51+925_51+926delinsTG	XP_016883625.1:n.51+925_51+926delinsTG
NM_001250.6:c.51+925_51+926delinsTG MANE Select	NP_001241.1:n.51+925_51+926delinsTG
NM_001302753.2:c.51+925_51+926delinsTG	NP_001289682.1:n.51+925_51+926delinsTG
NM_001322421.2:c.51+925_51+926delinsTG	NP_001309350.1:n.51+925_51+926delinsTG
NM_001322422.2:c.51+925_51+926delinsTG	NP_001309351.1:n.51+925_51+926delinsTG
NM_001362758.2:c.51+925_51+926delinsTG	NP_001349687.1:n.51+925_51+926delinsTG
NM_152854.4:c.51+925_51+926delinsTG	NP_690593.1:n.51+925_51+926delinsTG
NR_126502.2:n.81+925_81+926delinsTG
NR_136327.2:n.81+925_81+926delinsTG