Canonical Allele Identifier: CA409211644

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757548G>T (hg19) ; chr20:g.46128909G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128909G>T , CM000682.2:g.46128909G>T	GRCh38
NC_000020.10:g.44757548G>T , CM000682.1:g.44757548G>T	GRCh37
NC_000020.9:g.44190955G>T	NCBI36
NG_007279.1:g.15643G>T , LRG_40:g.15643G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.705G>T	ENSP00000512095.1:n.705G>T
ENST00000489304.6:c.786G>T	ENSP00000512096.1:n.786G>T
ENST00000695675.1:n.2579G>T
ENST00000372285.8:c.703G>T MANE Select	ENSP00000361359.3:p.Glu235Ter
ENST00000372276.7:c.*29G>T	ENSP00000361350.3:n.*29G>T
ENST00000372285.7:c.703G>T	ENSP00000361359.3:p.Glu235Ter
ENST00000466205.5:c.605G>T
ENST00000477696.5:n.676G>T
ENST00000489304.5:n.779G>T
ENST00000620709.4:c.*250G>T	ENSP00000484074.1:n.*250G>T
NM_001250.5:c.703G>T	NP_001241.1:p.Glu235Ter
NM_001302753.1:c.*29G>T	NP_001289682.1:n.*29G>T
NM_152854.3:c.*29G>T	NP_690593.1:n.*29G>T
NR_126502.1:n.796G>T
XM_005260617.2:c.715G>T	XP_005260674.1:p.Glu239Ter
XM_005260619.2:c.559G>T	XP_005260676.1:p.Glu187Ter
XR_936660.1:n.703G>T
NM_001322421.1:c.715G>T	NP_001309350.1:p.Glu239Ter
NM_001322422.1:c.547G>T	NP_001309351.1:p.Glu183Ter
NM_001362758.1:c.*29G>T	NP_001349687.1:n.*29G>T
NR_136327.1:n.699G>T
XM_005260619.3:c.559G>T	XP_005260676.1:p.Glu187Ter
XM_017028135.1:c.738G>T	XP_016883624.1:p.Arg246Ser
XM_017028136.1:c.636G>T	XP_016883625.1:p.Arg212Ser
NM_001250.6:c.703G>T MANE Select	NP_001241.1:p.Glu235Ter
NM_001302753.2:c.*29G>T	NP_001289682.1:n.*29G>T
NM_001322421.2:c.715G>T	NP_001309350.1:p.Glu239Ter
NM_001322422.2:c.547G>T	NP_001309351.1:p.Glu183Ter
NM_001362758.2:c.*29G>T	NP_001349687.1:n.*29G>T
NM_152854.4:c.*29G>T	NP_690593.1:n.*29G>T
NR_126502.2:n.736G>T
NR_136327.2:n.639G>T