Canonical Allele Identifier: CA510657867

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757640T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129001T>C , CM000682.2:g.46129001T>C	GRCh38
NC_000020.10:g.44757640T>C , CM000682.1:g.44757640T>C	GRCh37
NC_000020.9:g.44191047T>C	NCBI36
NG_007279.1:g.15735T>C , LRG_40:g.15735T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.797T>C	ENSP00000512095.1:n.797T>C
ENST00000489304.6:c.878T>C	ENSP00000512096.1:n.878T>C
ENST00000695675.1:n.2671T>C
ENST00000372285.8:c.795T>C MANE Select	ENSP00000361359.3:p.Asp265=
ENST00000372276.7:c.*121T>C	ENSP00000361350.3:n.*121T>C
ENST00000372285.7:c.795T>C	ENSP00000361359.3:p.Asp265=
ENST00000466205.5:c.697T>C
ENST00000477696.5:n.768T>C
ENST00000489304.5:n.871T>C
ENST00000620709.4:c.*342T>C	ENSP00000484074.1:n.*342T>C
NM_001250.5:c.795T>C	NP_001241.1:p.Asp265=
NM_001302753.1:c.*121T>C	NP_001289682.1:n.*121T>C
NM_152854.3:c.*121T>C	NP_690593.1:n.*121T>C
NR_126502.1:n.888T>C
XM_005260617.2:c.807T>C	XP_005260674.1:p.Asp269=
XM_005260619.2:c.651T>C	XP_005260676.1:p.Asp217=
XR_936660.1:n.795T>C
NM_001322421.1:c.807T>C	NP_001309350.1:p.Asp269=
NM_001322422.1:c.639T>C	NP_001309351.1:p.Asp213=
NM_001362758.1:c.*121T>C	NP_001349687.1:n.*121T>C
NR_136327.1:n.791T>C
XM_005260619.3:c.651T>C	XP_005260676.1:p.Asp217=
XM_017028135.1:c.830T>C	XP_016883624.1:p.Met277Thr
XM_017028136.1:c.728T>C	XP_016883625.1:p.Met243Thr
NM_001250.6:c.795T>C MANE Select	NP_001241.1:p.Asp265=
NM_001302753.2:c.*121T>C	NP_001289682.1:n.*121T>C
NM_001322421.2:c.807T>C	NP_001309350.1:p.Asp269=
NM_001322422.2:c.639T>C	NP_001309351.1:p.Asp213=
NM_001362758.2:c.*121T>C	NP_001349687.1:n.*121T>C
NM_152854.4:c.*121T>C	NP_690593.1:n.*121T>C
NR_126502.2:n.828T>C
NR_136327.2:n.731T>C