Canonical Allele Identifier: CA409205427

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44751348G>C (hg19) ; chr20:g.46122709G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46122709G>C , CM000682.2:g.46122709G>C	GRCh38
NC_000020.10:g.44751348G>C , CM000682.1:g.44751348G>C	GRCh37
NC_000020.9:g.44184755G>C	NCBI36
NG_007279.1:g.9443G>C , LRG_40:g.9443G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.452G>C	ENSP00000512095.1:n.452G>C
ENST00000489304.6:c.356G>C	ENSP00000512096.1:p.Cys119Ser
ENST00000695669.1:n.429G>C
ENST00000695670.1:n.336G>C
ENST00000695671.1:c.356G>C	ENSP00000512093.1:p.Cys119Ser
ENST00000695672.1:n.281G>C
ENST00000695673.1:n.221G>C
ENST00000372285.8:c.356G>C MANE Select	ENSP00000361359.3:p.Cys119Ser
ENST00000372276.7:c.356G>C	ENSP00000361350.3:p.Cys119Ser
ENST00000372285.7:c.356G>C	ENSP00000361359.3:p.Cys119Ser
ENST00000461171.1:n.141G>C
ENST00000466205.5:c.352G>C
ENST00000477696.5:n.423G>C
ENST00000489304.5:n.349G>C
ENST00000620709.4:c.356G>C	ENSP00000484074.1:p.Cys119Ser
NM_001250.5:c.356G>C	NP_001241.1:p.Cys119Ser
NM_001302753.1:c.356G>C	NP_001289682.1:p.Cys119Ser
NM_152854.3:c.356G>C	NP_690593.1:p.Cys119Ser
NR_126502.1:n.446G>C
XM_005260617.2:c.356G>C	XP_005260674.1:p.Cys119Ser
XM_005260619.2:c.356G>C	XP_005260676.1:p.Cys119Ser
XM_011529109.1:c.356G>C	XP_011527411.1:p.Cys119Ser
XR_936660.1:n.450G>C
NM_001322421.1:c.356G>C	NP_001309350.1:p.Cys119Ser
NM_001322422.1:c.356G>C	NP_001309351.1:p.Cys119Ser
NM_001362758.1:c.356G>C	NP_001349687.1:p.Cys119Ser
NR_136327.1:n.446G>C
XM_005260619.3:c.356G>C	XP_005260676.1:p.Cys119Ser
XM_011529109.2:c.356G>C	XP_011527411.1:p.Cys119Ser
XM_017028135.1:c.356G>C	XP_016883624.1:p.Cys119Ser
XM_017028136.1:c.356G>C	XP_016883625.1:p.Cys119Ser
NM_001250.6:c.356G>C MANE Select	NP_001241.1:p.Cys119Ser
NM_001302753.2:c.356G>C	NP_001289682.1:p.Cys119Ser
NM_001322421.2:c.356G>C	NP_001309350.1:p.Cys119Ser
NM_001322422.2:c.356G>C	NP_001309351.1:p.Cys119Ser
NM_001362758.2:c.356G>C	NP_001349687.1:p.Cys119Ser
NM_152854.4:c.356G>C	NP_690593.1:p.Cys119Ser
NR_126502.2:n.386G>C
NR_136327.2:n.386G>C