Canonical Allele Identifier: CA510657876

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757658C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129019C>A , CM000682.2:g.46129019C>A	GRCh38
NC_000020.10:g.44757658C>A , CM000682.1:g.44757658C>A	GRCh37
NC_000020.9:g.44191065C>A	NCBI36
NG_007279.1:g.15753C>A , LRG_40:g.15753C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.896C>A	ENSP00000512096.1:n.896C>A
ENST00000695675.1:n.2689C>A
ENST00000372285.8:c.813C>A MANE Select	ENSP00000361359.3:p.Ile271=
ENST00000372276.7:c.*139C>A	ENSP00000361350.3:n.*139C>A
ENST00000372285.7:c.813C>A	ENSP00000361359.3:p.Ile271=
ENST00000466205.5:c.715C>A
ENST00000489304.5:n.889C>A
ENST00000620709.4:c.*360C>A	ENSP00000484074.1:n.*360C>A
NM_001250.5:c.813C>A	NP_001241.1:p.Ile271=
NM_001302753.1:c.*139C>A	NP_001289682.1:n.*139C>A
NM_152854.3:c.*139C>A	NP_690593.1:n.*139C>A
NR_126502.1:n.906C>A
XM_005260617.2:c.825C>A	XP_005260674.1:p.Ile275=
XM_005260619.2:c.669C>A	XP_005260676.1:p.Ile223=
XR_936660.1:n.813C>A
NM_001322421.1:c.825C>A	NP_001309350.1:p.Ile275=
NM_001322422.1:c.657C>A	NP_001309351.1:p.Ile219=
NM_001362758.1:c.*139C>A	NP_001349687.1:n.*139C>A
NR_136327.1:n.809C>A
XM_005260619.3:c.669C>A	XP_005260676.1:p.Ile223=
XM_017028135.1:c.848C>A	XP_016883624.1:p.Ser283Tyr
XM_017028136.1:c.746C>A	XP_016883625.1:p.Ser249Tyr
NM_001250.6:c.813C>A MANE Select	NP_001241.1:p.Ile271=
NM_001302753.2:c.*139C>A	NP_001289682.1:n.*139C>A
NM_001322421.2:c.825C>A	NP_001309350.1:p.Ile275=
NM_001322422.2:c.657C>A	NP_001309351.1:p.Ile219=
NM_001362758.2:c.*139C>A	NP_001349687.1:n.*139C>A
NM_152854.4:c.*139C>A	NP_690593.1:n.*139C>A
NR_126502.2:n.846C>A
NR_136327.2:n.749C>A