Canonical Allele Identifier: CA2366533725

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128908G= , CM000682.2:g.46128908G=	GRCh38
NC_000020.10:g.44757547G= , CM000682.1:g.44757547G=	GRCh37
NC_000020.9:g.44190954G=	NCBI36
NG_007279.1:g.15642G= , LRG_40:g.15642G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.704G=	ENSP00000512095.1:n.704G=
ENST00000489304.6:c.785G=	ENSP00000512096.1:n.785G=
ENST00000695675.1:n.2578G=
ENST00000372285.8:c.702G= MANE Select	ENSP00000361359.3:p.Gln234=
ENST00000372276.7:c.*28G=	ENSP00000361350.3:n.*28G=
ENST00000372285.7:c.702G=	ENSP00000361359.3:p.Gln234=
ENST00000466205.5:c.604G=
ENST00000477696.5:n.675G=
ENST00000489304.5:n.778G=
ENST00000620709.4:c.*249G=	ENSP00000484074.1:n.*249G=
NM_001250.5:c.702G=	NP_001241.1:p.Gln234=
NM_001302753.1:c.*28G=	NP_001289682.1:n.*28G=
NM_152854.3:c.*28G=	NP_690593.1:n.*28G=
NR_126502.1:n.795G=
XM_005260617.2:c.714G=	XP_005260674.1:p.Gln238=
XM_005260619.2:c.558G=	XP_005260676.1:p.Gln186=
XR_936660.1:n.702G=
NM_001322421.1:c.714G=	NP_001309350.1:p.Gln238=
NM_001322422.1:c.546G=	NP_001309351.1:p.Gln182=
NM_001362758.1:c.*28G=	NP_001349687.1:n.*28G=
NR_136327.1:n.698G=
XM_005260619.3:c.558G=	XP_005260676.1:p.Gln186=
XM_017028135.1:c.737G=	XP_016883624.1:p.Arg246=
XM_017028136.1:c.635G=	XP_016883625.1:p.Arg212=
NM_001250.6:c.702G= MANE Select	NP_001241.1:p.Gln234=
NM_001302753.2:c.*28G=	NP_001289682.1:n.*28G=
NM_001322421.2:c.714G=	NP_001309350.1:p.Gln238=
NM_001322422.2:c.546G=	NP_001309351.1:p.Gln182=
NM_001362758.2:c.*28G=	NP_001349687.1:n.*28G=
NM_152854.4:c.*28G=	NP_690593.1:n.*28G=
NR_126502.2:n.735G=
NR_136327.2:n.638G=