Canonical Allele Identifier: CA2366530740

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46122641C= , CM000682.2:g.46122641C=	GRCh38
NC_000020.10:g.44751280C= , CM000682.1:g.44751280C=	GRCh37
NC_000020.9:g.44184687C=	NCBI36
NG_007279.1:g.9375C= , LRG_40:g.9375C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.384C=	ENSP00000512095.1:n.384C=
ENST00000489304.6:c.288C=	ENSP00000512096.1:p.Thr96=
ENST00000695669.1:n.361C=
ENST00000695670.1:n.268C=
ENST00000695671.1:c.288C=	ENSP00000512093.1:p.Thr96=
ENST00000695672.1:n.213C=
ENST00000695673.1:n.153C=
ENST00000372285.8:c.288C= MANE Select	ENSP00000361359.3:p.Thr96=
ENST00000372276.7:c.288C=	ENSP00000361350.3:p.Thr96=
ENST00000372285.7:c.288C=	ENSP00000361359.3:p.Thr96=
ENST00000461171.1:n.73C=
ENST00000466205.5:c.284C=
ENST00000477696.5:n.355C=
ENST00000489304.5:n.281C=
ENST00000620709.4:c.288C=	ENSP00000484074.1:p.Thr96=
NM_001250.5:c.288C=	NP_001241.1:p.Thr96=
NM_001302753.1:c.288C=	NP_001289682.1:p.Thr96=
NM_152854.3:c.288C=	NP_690593.1:p.Thr96=
NR_126502.1:n.378C=
XM_005260617.2:c.288C=	XP_005260674.1:p.Thr96=
XM_005260619.2:c.288C=	XP_005260676.1:p.Thr96=
XM_011529109.1:c.288C=	XP_011527411.1:p.Thr96=
XR_936660.1:n.382C=
NM_001322421.1:c.288C=	NP_001309350.1:p.Thr96=
NM_001322422.1:c.288C=	NP_001309351.1:p.Thr96=
NM_001362758.1:c.288C=	NP_001349687.1:p.Thr96=
NR_136327.1:n.378C=
XM_005260619.3:c.288C=	XP_005260676.1:p.Thr96=
XM_011529109.2:c.288C=	XP_011527411.1:p.Thr96=
XM_017028135.1:c.288C=	XP_016883624.1:p.Thr96=
XM_017028136.1:c.288C=	XP_016883625.1:p.Thr96=
NM_001250.6:c.288C= MANE Select	NP_001241.1:p.Thr96=
NM_001302753.2:c.288C=	NP_001289682.1:p.Thr96=
NM_001322421.2:c.288C=	NP_001309350.1:p.Thr96=
NM_001322422.2:c.288C=	NP_001309351.1:p.Thr96=
NM_001362758.2:c.288C=	NP_001349687.1:p.Thr96=
NM_152854.4:c.288C=	NP_690593.1:p.Thr96=
NR_126502.2:n.318C=
NR_136327.2:n.318C=