Canonical Allele Identifier: CA409211743

Gene: CD40

Linked Data

• COSMIC: COSM3547205
• MyVariant Identifiers: chr20:g.44757560C>T (hg19) ; chr20:g.46128921C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128921C>T , CM000682.2:g.46128921C>T	GRCh38
NC_000020.10:g.44757560C>T , CM000682.1:g.44757560C>T	GRCh37
NC_000020.9:g.44190967C>T	NCBI36
NG_007279.1:g.15655C>T , LRG_40:g.15655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.717C>T	ENSP00000512095.1:n.717C>T
ENST00000489304.6:c.798C>T	ENSP00000512096.1:n.798C>T
ENST00000695675.1:n.2591C>T
ENST00000372285.8:c.715C>T MANE Select	ENSP00000361359.3:p.Pro239Ser
ENST00000372276.7:c.*41C>T	ENSP00000361350.3:n.*41C>T
ENST00000372285.7:c.715C>T	ENSP00000361359.3:p.Pro239Ser
ENST00000466205.5:c.617C>T
ENST00000477696.5:n.688C>T
ENST00000489304.5:n.791C>T
ENST00000620709.4:c.*262C>T	ENSP00000484074.1:n.*262C>T
NM_001250.5:c.715C>T	NP_001241.1:p.Pro239Ser
NM_001302753.1:c.*41C>T	NP_001289682.1:n.*41C>T
NM_152854.3:c.*41C>T	NP_690593.1:n.*41C>T
NR_126502.1:n.808C>T
XM_005260617.2:c.727C>T	XP_005260674.1:p.Pro243Ser
XM_005260619.2:c.571C>T	XP_005260676.1:p.Pro191Ser
XR_936660.1:n.715C>T
NM_001322421.1:c.727C>T	NP_001309350.1:p.Pro243Ser
NM_001322422.1:c.559C>T	NP_001309351.1:p.Pro187Ser
NM_001362758.1:c.*41C>T	NP_001349687.1:n.*41C>T
NR_136327.1:n.711C>T
XM_005260619.3:c.571C>T	XP_005260676.1:p.Pro191Ser
XM_017028135.1:c.750C>T	XP_016883624.1:p.Phe250=
XM_017028136.1:c.648C>T	XP_016883625.1:p.Phe216=
NM_001250.6:c.715C>T MANE Select	NP_001241.1:p.Pro239Ser
NM_001302753.2:c.*41C>T	NP_001289682.1:n.*41C>T
NM_001322421.2:c.727C>T	NP_001309350.1:p.Pro243Ser
NM_001322422.2:c.559C>T	NP_001309351.1:p.Pro187Ser
NM_001362758.2:c.*41C>T	NP_001349687.1:n.*41C>T
NM_152854.4:c.*41C>T	NP_690593.1:n.*41C>T
NR_126502.2:n.748C>T
NR_136327.2:n.651C>T