Canonical Allele Identifier: CA2737036738

Gene: CD40

Linked Data

• dbSNP Id: rs2145615358

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128789G>C , CM000682.2:g.46128789G>C	GRCh38
NC_000020.10:g.44757428G>C , CM000682.1:g.44757428G>C	GRCh37
NC_000020.9:g.44190835G>C	NCBI36
NG_007279.1:g.15523G>C , LRG_40:g.15523G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.678-93G>C	ENSP00000512095.1:n.678-93G>C
ENST00000489304.6:c.759-93G>C	ENSP00000512096.1:n.759-93G>C
ENST00000695675.1:n.2552-93G>C
ENST00000372285.8:c.676-93G>C MANE Select	ENSP00000361359.3:n.676-93G>C
ENST00000372276.7:c.*2-93G>C	ENSP00000361350.3:n.*2-93G>C
ENST00000372285.7:c.676-93G>C	ENSP00000361359.3:n.676-93G>C
ENST00000466205.5:c.578-93G>C
ENST00000477696.5:n.649-93G>C
ENST00000489304.5:n.752-93G>C
ENST00000620709.4:c.*223-93G>C	ENSP00000484074.1:n.*223-93G>C
NM_001250.5:c.676-93G>C	NP_001241.1:n.676-93G>C
NM_001302753.1:c.*2-93G>C	NP_001289682.1:n.*2-93G>C
NM_152854.3:c.*2-93G>C	NP_690593.1:n.*2-93G>C
NR_126502.1:n.769-93G>C
XM_005260617.2:c.688-93G>C	XP_005260674.1:n.688-93G>C
XM_005260619.2:c.532-93G>C	XP_005260676.1:n.532-93G>C
XR_936660.1:n.676-93G>C
NM_001322421.1:c.688-93G>C	NP_001309350.1:n.688-93G>C
NM_001322422.1:c.520-93G>C	NP_001309351.1:n.520-93G>C
NM_001362758.1:c.*2-93G>C	NP_001349687.1:n.*2-93G>C
NR_136327.1:n.672-93G>C
XM_005260619.3:c.532-93G>C	XP_005260676.1:n.532-93G>C
XM_017028135.1:c.711-93G>C	XP_016883624.1:n.711-93G>C
XM_017028136.1:c.609-93G>C	XP_016883625.1:n.609-93G>C
NM_001250.6:c.676-93G>C MANE Select	NP_001241.1:n.676-93G>C
NM_001302753.2:c.*2-93G>C	NP_001289682.1:n.*2-93G>C
NM_001322421.2:c.688-93G>C	NP_001309350.1:n.688-93G>C
NM_001322422.2:c.520-93G>C	NP_001309351.1:n.520-93G>C
NM_001362758.2:c.*2-93G>C	NP_001349687.1:n.*2-93G>C
NM_152854.4:c.*2-93G>C	NP_690593.1:n.*2-93G>C
NR_126502.2:n.709-93G>C
NR_136327.2:n.612-93G>C