Canonical Allele Identifier: CA409200441

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44746995C>G (hg19) ; chr20:g.46118356C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46118356C>G , CM000682.2:g.46118356C>G	GRCh38
NC_000020.10:g.44746995C>G , CM000682.1:g.44746995C>G	GRCh37
NC_000020.9:g.44180402C>G	NCBI36
NG_007279.1:g.5090C>G , LRG_40:g.5090C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.13C>G	ENSP00000512095.1:p.Pro5Ala
ENST00000489304.6:c.13C>G	ENSP00000512096.1:p.Pro5Ala
ENST00000695669.1:n.86C>G
ENST00000695670.1:n.72C>G
ENST00000695671.1:c.13C>G	ENSP00000512093.1:p.Pro5Ala
ENST00000695672.1:n.17C>G
ENST00000372285.8:c.13C>G MANE Select	ENSP00000361359.3:p.Pro5Ala
ENST00000372276.7:c.13C>G	ENSP00000361350.3:p.Pro5Ala
ENST00000372285.7:c.13C>G	ENSP00000361359.3:p.Pro5Ala
ENST00000466205.5:c.9C>G
ENST00000489304.5:n.6C>G
ENST00000620709.4:c.13C>G	ENSP00000484074.1:p.Pro5Ala
NM_001250.5:c.13C>G	NP_001241.1:p.Pro5Ala
NM_001302753.1:c.13C>G	NP_001289682.1:p.Pro5Ala
NM_152854.3:c.13C>G	NP_690593.1:p.Pro5Ala
NR_126502.1:n.103C>G
XM_005260617.2:c.13C>G	XP_005260674.1:p.Pro5Ala
XM_005260619.2:c.13C>G	XP_005260676.1:p.Pro5Ala
XM_011529109.1:c.13C>G	XP_011527411.1:p.Pro5Ala
XR_936660.1:n.107C>G
NM_001322421.1:c.13C>G	NP_001309350.1:p.Pro5Ala
NM_001322422.1:c.13C>G	NP_001309351.1:p.Pro5Ala
NM_001362758.1:c.13C>G	NP_001349687.1:p.Pro5Ala
NR_136327.1:n.103C>G
XM_005260619.3:c.13C>G	XP_005260676.1:p.Pro5Ala
XM_011529109.2:c.13C>G	XP_011527411.1:p.Pro5Ala
XM_017028135.1:c.13C>G	XP_016883624.1:p.Pro5Ala
XM_017028136.1:c.13C>G	XP_016883625.1:p.Pro5Ala
NM_001250.6:c.13C>G MANE Select	NP_001241.1:p.Pro5Ala
NM_001302753.2:c.13C>G	NP_001289682.1:p.Pro5Ala
NM_001322421.2:c.13C>G	NP_001309350.1:p.Pro5Ala
NM_001322422.2:c.13C>G	NP_001309351.1:p.Pro5Ala
NM_001362758.2:c.13C>G	NP_001349687.1:p.Pro5Ala
NM_152854.4:c.13C>G	NP_690593.1:p.Pro5Ala
NR_126502.2:n.43C>G
NR_136327.2:n.43C>G