Canonical Allele Identifier: CA409212347

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757659T>C (hg19) ; chr20:g.46129020T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129020T>C , CM000682.2:g.46129020T>C	GRCh38
NC_000020.10:g.44757659T>C , CM000682.1:g.44757659T>C	GRCh37
NC_000020.9:g.44191066T>C	NCBI36
NG_007279.1:g.15754T>C , LRG_40:g.15754T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.897T>C	ENSP00000512096.1:n.897T>C
ENST00000695675.1:n.2690T>C
ENST00000372285.8:c.814T>C MANE Select	ENSP00000361359.3:p.Ser272Pro
ENST00000372276.7:c.*140T>C	ENSP00000361350.3:n.*140T>C
ENST00000372285.7:c.814T>C	ENSP00000361359.3:p.Ser272Pro
ENST00000466205.5:c.716T>C
ENST00000489304.5:n.890T>C
ENST00000620709.4:c.*361T>C	ENSP00000484074.1:n.*361T>C
NM_001250.5:c.814T>C	NP_001241.1:p.Ser272Pro
NM_001302753.1:c.*140T>C	NP_001289682.1:n.*140T>C
NM_152854.3:c.*140T>C	NP_690593.1:n.*140T>C
NR_126502.1:n.907T>C
XM_005260617.2:c.826T>C	XP_005260674.1:p.Ser276Pro
XM_005260619.2:c.670T>C	XP_005260676.1:p.Ser224Pro
XR_936660.1:n.814T>C
NM_001322421.1:c.826T>C	NP_001309350.1:p.Ser276Pro
NM_001322422.1:c.658T>C	NP_001309351.1:p.Ser220Pro
NM_001362758.1:c.*140T>C	NP_001349687.1:n.*140T>C
NR_136327.1:n.810T>C
XM_005260619.3:c.670T>C	XP_005260676.1:p.Ser224Pro
XM_017028135.1:c.849T>C	XP_016883624.1:p.Ser283=
XM_017028136.1:c.747T>C	XP_016883625.1:p.Ser249=
NM_001250.6:c.814T>C MANE Select	NP_001241.1:p.Ser272Pro
NM_001302753.2:c.*140T>C	NP_001289682.1:n.*140T>C
NM_001322421.2:c.826T>C	NP_001309350.1:p.Ser276Pro
NM_001322422.2:c.658T>C	NP_001309351.1:p.Ser220Pro
NM_001362758.2:c.*140T>C	NP_001349687.1:n.*140T>C
NM_152854.4:c.*140T>C	NP_690593.1:n.*140T>C
NR_126502.2:n.847T>C
NR_136327.2:n.750T>C