Canonical Allele Identifier: CA409212215

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757639A>T (hg19) ; chr20:g.46129000A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129000A>T , CM000682.2:g.46129000A>T	GRCh38
NC_000020.10:g.44757639A>T , CM000682.1:g.44757639A>T	GRCh37
NC_000020.9:g.44191046A>T	NCBI36
NG_007279.1:g.15734A>T , LRG_40:g.15734A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.796A>T	ENSP00000512095.1:n.796A>T
ENST00000489304.6:c.877A>T	ENSP00000512096.1:n.877A>T
ENST00000695675.1:n.2670A>T
ENST00000372285.8:c.794A>T MANE Select	ENSP00000361359.3:p.Asp265Val
ENST00000372276.7:c.*120A>T	ENSP00000361350.3:n.*120A>T
ENST00000372285.7:c.794A>T	ENSP00000361359.3:p.Asp265Val
ENST00000466205.5:c.696A>T
ENST00000477696.5:n.767A>T
ENST00000489304.5:n.870A>T
ENST00000620709.4:c.*341A>T	ENSP00000484074.1:n.*341A>T
NM_001250.5:c.794A>T	NP_001241.1:p.Asp265Val
NM_001302753.1:c.*120A>T	NP_001289682.1:n.*120A>T
NM_152854.3:c.*120A>T	NP_690593.1:n.*120A>T
NR_126502.1:n.887A>T
XM_005260617.2:c.806A>T	XP_005260674.1:p.Asp269Val
XM_005260619.2:c.650A>T	XP_005260676.1:p.Asp217Val
XR_936660.1:n.794A>T
NM_001322421.1:c.806A>T	NP_001309350.1:p.Asp269Val
NM_001322422.1:c.638A>T	NP_001309351.1:p.Asp213Val
NM_001362758.1:c.*120A>T	NP_001349687.1:n.*120A>T
NR_136327.1:n.790A>T
XM_005260619.3:c.650A>T	XP_005260676.1:p.Asp217Val
XM_017028135.1:c.829A>T	XP_016883624.1:p.Met277Leu
XM_017028136.1:c.727A>T	XP_016883625.1:p.Met243Leu
NM_001250.6:c.794A>T MANE Select	NP_001241.1:p.Asp265Val
NM_001302753.2:c.*120A>T	NP_001289682.1:n.*120A>T
NM_001322421.2:c.806A>T	NP_001309350.1:p.Asp269Val
NM_001322422.2:c.638A>T	NP_001309351.1:p.Asp213Val
NM_001362758.2:c.*120A>T	NP_001349687.1:n.*120A>T
NM_152854.4:c.*120A>T	NP_690593.1:n.*120A>T
NR_126502.2:n.827A>T
NR_136327.2:n.730A>T