Canonical Allele Identifier: CA409212240

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757644A>C (hg19) ; chr20:g.46129005A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129005A>C , CM000682.2:g.46129005A>C	GRCh38
NC_000020.10:g.44757644A>C , CM000682.1:g.44757644A>C	GRCh37
NC_000020.9:g.44191051A>C	NCBI36
NG_007279.1:g.15739A>C , LRG_40:g.15739A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.882A>C	ENSP00000512096.1:n.882A>C
ENST00000695675.1:n.2675A>C
ENST00000372285.8:c.799A>C MANE Select	ENSP00000361359.3:p.Lys267Gln
ENST00000372276.7:c.*125A>C	ENSP00000361350.3:n.*125A>C
ENST00000372285.7:c.799A>C	ENSP00000361359.3:p.Lys267Gln
ENST00000466205.5:c.701A>C
ENST00000489304.5:n.875A>C
ENST00000620709.4:c.*346A>C	ENSP00000484074.1:n.*346A>C
NM_001250.5:c.799A>C	NP_001241.1:p.Lys267Gln
NM_001302753.1:c.*125A>C	NP_001289682.1:n.*125A>C
NM_152854.3:c.*125A>C	NP_690593.1:n.*125A>C
NR_126502.1:n.892A>C
XM_005260617.2:c.811A>C	XP_005260674.1:p.Lys271Gln
XM_005260619.2:c.655A>C	XP_005260676.1:p.Lys219Gln
XR_936660.1:n.799A>C
NM_001322421.1:c.811A>C	NP_001309350.1:p.Lys271Gln
NM_001322422.1:c.643A>C	NP_001309351.1:p.Lys215Gln
NM_001362758.1:c.*125A>C	NP_001349687.1:n.*125A>C
NR_136327.1:n.795A>C
XM_005260619.3:c.655A>C	XP_005260676.1:p.Lys219Gln
XM_017028135.1:c.834A>C	XP_016883624.1:p.Ala278=
XM_017028136.1:c.732A>C	XP_016883625.1:p.Ala244=
NM_001250.6:c.799A>C MANE Select	NP_001241.1:p.Lys267Gln
NM_001302753.2:c.*125A>C	NP_001289682.1:n.*125A>C
NM_001322421.2:c.811A>C	NP_001309350.1:p.Lys271Gln
NM_001322422.2:c.643A>C	NP_001309351.1:p.Lys215Gln
NM_001362758.2:c.*125A>C	NP_001349687.1:n.*125A>C
NM_152854.4:c.*125A>C	NP_690593.1:n.*125A>C
NR_126502.2:n.832A>C
NR_136327.2:n.735A>C