Canonical Allele Identifier: CA2366533656

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128791_46128792delinsCT , CM000682.2:g.46128791_46128792delinsCT	GRCh38
NC_000020.10:g.44757430_44757431delinsCT , CM000682.1:g.44757430_44757431delinsCT	GRCh37
NC_000020.9:g.44190837_44190838delinsCT	NCBI36
NG_007279.1:g.15525_15526delinsCT , LRG_40:g.15525_15526delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.678-91_678-90delinsCT	ENSP00000512095.1:n.678-91_678-90delinsCT...
ENST00000489304.6:c.759-91_759-90delinsCT	ENSP00000512096.1:n.759-91_759-90delinsCT...
ENST00000695675.1:n.2552-91_2552-90delinsCT
ENST00000372285.8:c.676-91_676-90delinsCT MANE Select	ENSP00000361359.3:n.676-91_676-90delinsCT...
ENST00000372276.7:c.*2-91_*2-90delinsCT	ENSP00000361350.3:n.*2-91_*2-90delinsCT
ENST00000372285.7:c.676-91_676-90delinsCT	ENSP00000361359.3:n.676-91_676-90delinsCT...
ENST00000466205.5:c.578-91_578-90delinsCT
ENST00000477696.5:n.649-91_649-90delinsCT
ENST00000489304.5:n.752-91_752-90delinsCT
ENST00000620709.4:c.*223-91_*223-90delinsCT	ENSP00000484074.1:n.*223-91_*223-90delins...
NM_001250.5:c.676-91_676-90delinsCT	NP_001241.1:n.676-91_676-90delinsCT
NM_001302753.1:c.*2-91_*2-90delinsCT	NP_001289682.1:n.*2-91_*2-90delinsCT
NM_152854.3:c.*2-91_*2-90delinsCT	NP_690593.1:n.*2-91_*2-90delinsCT
NR_126502.1:n.769-91_769-90delinsCT
XM_005260617.2:c.688-91_688-90delinsCT	XP_005260674.1:n.688-91_688-90delinsCT
XM_005260619.2:c.532-91_532-90delinsCT	XP_005260676.1:n.532-91_532-90delinsCT
XR_936660.1:n.676-91_676-90delinsCT
NM_001322421.1:c.688-91_688-90delinsCT	NP_001309350.1:n.688-91_688-90delinsCT
NM_001322422.1:c.520-91_520-90delinsCT	NP_001309351.1:n.520-91_520-90delinsCT
NM_001362758.1:c.*2-91_*2-90delinsCT	NP_001349687.1:n.*2-91_*2-90delinsCT
NR_136327.1:n.672-91_672-90delinsCT
XM_005260619.3:c.532-91_532-90delinsCT	XP_005260676.1:n.532-91_532-90delinsCT
XM_017028135.1:c.711-91_711-90delinsCT	XP_016883624.1:n.711-91_711-90delinsCT
XM_017028136.1:c.609-91_609-90delinsCT	XP_016883625.1:n.609-91_609-90delinsCT
NM_001250.6:c.676-91_676-90delinsCT MANE Select	NP_001241.1:n.676-91_676-90delinsCT
NM_001302753.2:c.*2-91_*2-90delinsCT	NP_001289682.1:n.*2-91_*2-90delinsCT
NM_001322421.2:c.688-91_688-90delinsCT	NP_001309350.1:n.688-91_688-90delinsCT
NM_001322422.2:c.520-91_520-90delinsCT	NP_001309351.1:n.520-91_520-90delinsCT
NM_001362758.2:c.*2-91_*2-90delinsCT	NP_001349687.1:n.*2-91_*2-90delinsCT
NM_152854.4:c.*2-91_*2-90delinsCT	NP_690593.1:n.*2-91_*2-90delinsCT
NR_126502.2:n.709-91_709-90delinsCT
NR_136327.2:n.612-91_612-90delinsCT