Canonical Allele Identifier: CA409211512

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757529C>G (hg19) ; chr20:g.46128890C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128890C>G , CM000682.2:g.46128890C>G	GRCh38
NC_000020.10:g.44757529C>G , CM000682.1:g.44757529C>G	GRCh37
NC_000020.9:g.44190936C>G	NCBI36
NG_007279.1:g.15624C>G , LRG_40:g.15624C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.686C>G	ENSP00000512095.1:n.686C>G
ENST00000489304.6:c.767C>G	ENSP00000512096.1:n.767C>G
ENST00000695675.1:n.2560C>G
ENST00000372285.8:c.684C>G MANE Select	ENSP00000361359.3:p.His228Gln
ENST00000372276.7:c.*10C>G	ENSP00000361350.3:n.*10C>G
ENST00000372285.7:c.684C>G	ENSP00000361359.3:p.His228Gln
ENST00000466205.5:c.586C>G
ENST00000477696.5:n.657C>G
ENST00000489304.5:n.760C>G
ENST00000620709.4:c.*231C>G	ENSP00000484074.1:n.*231C>G
NM_001250.5:c.684C>G	NP_001241.1:p.His228Gln
NM_001302753.1:c.*10C>G	NP_001289682.1:n.*10C>G
NM_152854.3:c.*10C>G	NP_690593.1:n.*10C>G
NR_126502.1:n.777C>G
XM_005260617.2:c.696C>G	XP_005260674.1:p.His232Gln
XM_005260619.2:c.540C>G	XP_005260676.1:p.His180Gln
XR_936660.1:n.684C>G
NM_001322421.1:c.696C>G	NP_001309350.1:p.His232Gln
NM_001322422.1:c.528C>G	NP_001309351.1:p.His176Gln
NM_001362758.1:c.*10C>G	NP_001349687.1:n.*10C>G
NR_136327.1:n.680C>G
XM_005260619.3:c.540C>G	XP_005260676.1:p.His180Gln
XM_017028135.1:c.719C>G	XP_016883624.1:p.Thr240Ser
XM_017028136.1:c.617C>G	XP_016883625.1:p.Thr206Ser
NM_001250.6:c.684C>G MANE Select	NP_001241.1:p.His228Gln
NM_001302753.2:c.*10C>G	NP_001289682.1:n.*10C>G
NM_001322421.2:c.696C>G	NP_001309350.1:p.His232Gln
NM_001322422.2:c.528C>G	NP_001309351.1:p.His176Gln
NM_001362758.2:c.*10C>G	NP_001349687.1:n.*10C>G
NM_152854.4:c.*10C>G	NP_690593.1:n.*10C>G
NR_126502.2:n.717C>G
NR_136327.2:n.620C>G