Canonical Allele Identifier: CA2366533192

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129015G= , CM000682.2:g.46129015G=	GRCh38
NC_000020.10:g.44757654G= , CM000682.1:g.44757654G=	GRCh37
NC_000020.9:g.44191061G=	NCBI36
NG_007279.1:g.15749G= , LRG_40:g.15749G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.892G=	ENSP00000512096.1:n.892G=
ENST00000695675.1:n.2685G=
ENST00000372285.8:c.809G= MANE Select	ENSP00000361359.3:p.Arg270=
ENST00000372276.7:c.*135G=	ENSP00000361350.3:n.*135G=
ENST00000372285.7:c.809G=	ENSP00000361359.3:p.Arg270=
ENST00000466205.5:c.711G=
ENST00000489304.5:n.885G=
ENST00000620709.4:c.*356G=	ENSP00000484074.1:n.*356G=
NM_001250.5:c.809G=	NP_001241.1:p.Arg270=
NM_001302753.1:c.*135G=	NP_001289682.1:n.*135G=
NM_152854.3:c.*135G=	NP_690593.1:n.*135G=
NR_126502.1:n.902G=
XM_005260617.2:c.821G=	XP_005260674.1:p.Arg274=
XM_005260619.2:c.665G=	XP_005260676.1:p.Arg222=
XR_936660.1:n.809G=
NM_001322421.1:c.821G=	NP_001309350.1:p.Arg274=
NM_001322422.1:c.653G=	NP_001309351.1:p.Arg218=
NM_001362758.1:c.*135G=	NP_001349687.1:n.*135G=
NR_136327.1:n.805G=
XM_005260619.3:c.665G=	XP_005260676.1:p.Arg222=
XM_017028135.1:c.844G=	XP_016883624.1:p.Ala282=
XM_017028136.1:c.742G=	XP_016883625.1:p.Ala248=
NM_001250.6:c.809G= MANE Select	NP_001241.1:p.Arg270=
NM_001302753.2:c.*135G=	NP_001289682.1:n.*135G=
NM_001322421.2:c.821G=	NP_001309350.1:p.Arg274=
NM_001322422.2:c.653G=	NP_001309351.1:p.Arg218=
NM_001362758.2:c.*135G=	NP_001349687.1:n.*135G=
NM_152854.4:c.*135G=	NP_690593.1:n.*135G=
NR_126502.2:n.842G=
NR_136327.2:n.745G=