Canonical Allele Identifier: CA409209057

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44756796A>G (hg19) ; chr20:g.46128157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128157A>G , CM000682.2:g.46128157A>G	GRCh38
NC_000020.10:g.44756796A>G , CM000682.1:g.44756796A>G	GRCh37
NC_000020.9:g.44190203A>G	NCBI36
NG_007279.1:g.14891A>G , LRG_40:g.14891A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.581A>G	ENSP00000512095.1:n.581A>G
ENST00000489304.6:c.662A>G	ENSP00000512096.1:n.662A>G
ENST00000695670.1:n.548A>G
ENST00000695671.1:c.619A>G	ENSP00000512093.1:p.Ser207Gly
ENST00000695674.1:n.1058A>G
ENST00000695675.1:n.2455A>G
ENST00000372285.8:c.579A>G MANE Select	ENSP00000361359.3:p.Arg193=
ENST00000372276.7:c.517A>G	ENSP00000361350.3:p.Ser173Gly
ENST00000372285.7:c.579A>G	ENSP00000361359.3:p.Arg193=
ENST00000466205.5:c.481A>G
ENST00000477696.5:n.552A>G
ENST00000489304.5:n.655A>G
ENST00000620709.4:c.*126A>G	ENSP00000484074.1:n.*126A>G
NM_001250.5:c.579A>G	NP_001241.1:p.Arg193=
NM_001302753.1:c.619A>G	NP_001289682.1:p.Ser207Gly
NM_152854.3:c.517A>G	NP_690593.1:p.Ser173Gly
NR_126502.1:n.672A>G
XM_005260617.2:c.579A>G	XP_005260674.1:p.Arg193=
XM_005260619.2:c.423A>G	XP_005260676.1:p.Arg141=
XR_936660.1:n.579A>G
NM_001322421.1:c.579A>G	NP_001309350.1:p.Arg193=
NM_001322422.1:c.423A>G	NP_001309351.1:p.Arg141=
NM_001362758.1:c.579A>G	NP_001349687.1:p.Arg193=
NR_136327.1:n.575A>G
XM_005260619.3:c.423A>G	XP_005260676.1:p.Arg141=
XM_017028135.1:c.619A>G	XP_016883624.1:p.Ser207Gly
XM_017028136.1:c.517A>G	XP_016883625.1:p.Ser173Gly
NM_001250.6:c.579A>G MANE Select	NP_001241.1:p.Arg193=
NM_001302753.2:c.619A>G	NP_001289682.1:p.Ser207Gly
NM_001322421.2:c.579A>G	NP_001309350.1:p.Arg193=
NM_001322422.2:c.423A>G	NP_001309351.1:p.Arg141=
NM_001362758.2:c.579A>G	NP_001349687.1:p.Arg193=
NM_152854.4:c.517A>G	NP_690593.1:p.Ser173Gly
NR_126502.2:n.612A>G
NR_136327.2:n.515A>G