Canonical Allele Identifier: CA409212221

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757640T>G (hg19) ; chr20:g.46129001T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.797T>G	ENSP00000512095.1:n.797T>G
ENST00000489304.6:c.878T>G	ENSP00000512096.1:n.878T>G
ENST00000695675.1:n.2671T>G
ENST00000372285.8:c.795T>G MANE Select	ENSP00000361359.3:p.Asp265Glu
ENST00000372276.7:c.*121T>G	ENSP00000361350.3:n.*121T>G
ENST00000372285.7:c.795T>G	ENSP00000361359.3:p.Asp265Glu
ENST00000466205.5:c.697T>G
ENST00000477696.5:n.768T>G
ENST00000489304.5:n.871T>G
ENST00000620709.4:c.*342T>G	ENSP00000484074.1:n.*342T>G
NM_001250.5:c.795T>G	NP_001241.1:p.Asp265Glu
NM_001302753.1:c.*121T>G	NP_001289682.1:n.*121T>G
NM_152854.3:c.*121T>G	NP_690593.1:n.*121T>G
NR_126502.1:n.888T>G
XM_005260617.2:c.807T>G	XP_005260674.1:p.Asp269Glu
XM_005260619.2:c.651T>G	XP_005260676.1:p.Asp217Glu
XR_936660.1:n.795T>G
NM_001322421.1:c.807T>G	NP_001309350.1:p.Asp269Glu
NM_001322422.1:c.639T>G	NP_001309351.1:p.Asp213Glu
NM_001362758.1:c.*121T>G	NP_001349687.1:n.*121T>G
NR_136327.1:n.791T>G
XM_005260619.3:c.651T>G	XP_005260676.1:p.Asp217Glu
XM_017028135.1:c.830T>G	XP_016883624.1:p.Met277Arg
XM_017028136.1:c.728T>G	XP_016883625.1:p.Met243Arg
NM_001250.6:c.795T>G MANE Select	NP_001241.1:p.Asp265Glu
NM_001302753.2:c.*121T>G	NP_001289682.1:n.*121T>G
NM_001322421.2:c.807T>G	NP_001309350.1:p.Asp269Glu
NM_001322422.2:c.639T>G	NP_001309351.1:p.Asp213Glu
NM_001362758.2:c.*121T>G	NP_001349687.1:n.*121T>G
NM_152854.4:c.*121T>G	NP_690593.1:n.*121T>G
NR_126502.2:n.828T>G
NR_136327.2:n.731T>G