Canonical Allele Identifier: CA2366533726

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128916A= , CM000682.2:g.46128916A=	GRCh38
NC_000020.10:g.44757555A= , CM000682.1:g.44757555A=	GRCh37
NC_000020.9:g.44190962A=	NCBI36
NG_007279.1:g.15650A= , LRG_40:g.15650A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.712A=	ENSP00000512095.1:n.712A=
ENST00000489304.6:c.793A=	ENSP00000512096.1:n.793A=
ENST00000695675.1:n.2586A=
ENST00000372285.8:c.710A= MANE Select	ENSP00000361359.3:p.Asn237=
ENST00000372276.7:c.*36A=	ENSP00000361350.3:n.*36A=
ENST00000372285.7:c.710A=	ENSP00000361359.3:p.Asn237=
ENST00000466205.5:c.612A=
ENST00000477696.5:n.683A=
ENST00000489304.5:n.786A=
ENST00000620709.4:c.*257A=	ENSP00000484074.1:n.*257A=
NM_001250.5:c.710A=	NP_001241.1:p.Asn237=
NM_001302753.1:c.*36A=	NP_001289682.1:n.*36A=
NM_152854.3:c.*36A=	NP_690593.1:n.*36A=
NR_126502.1:n.803A=
XM_005260617.2:c.722A=	XP_005260674.1:p.Asn241=
XM_005260619.2:c.566A=	XP_005260676.1:p.Asn189=
XR_936660.1:n.710A=
NM_001322421.1:c.722A=	NP_001309350.1:p.Asn241=
NM_001322422.1:c.554A=	NP_001309351.1:p.Asn185=
NM_001362758.1:c.*36A=	NP_001349687.1:n.*36A=
NR_136327.1:n.706A=
XM_005260619.3:c.566A=	XP_005260676.1:p.Asn189=
XM_017028135.1:c.745A=	XP_016883624.1:p.Ile249=
XM_017028136.1:c.643A=	XP_016883625.1:p.Ile215=
NM_001250.6:c.710A= MANE Select	NP_001241.1:p.Asn237=
NM_001302753.2:c.*36A=	NP_001289682.1:n.*36A=
NM_001322421.2:c.722A=	NP_001309350.1:p.Asn241=
NM_001322422.2:c.554A=	NP_001309351.1:p.Asn185=
NM_001362758.2:c.*36A=	NP_001349687.1:n.*36A=
NM_152854.4:c.*36A=	NP_690593.1:n.*36A=
NR_126502.2:n.743A=
NR_136327.2:n.646A=