Canonical Allele Identifier: CA409209614

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44756860A>G (hg19) ; chr20:g.46128221A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128221A>G , CM000682.2:g.46128221A>G	GRCh38
NC_000020.10:g.44756860A>G , CM000682.1:g.44756860A>G	GRCh37
NC_000020.9:g.44190267A>G	NCBI36
NG_007279.1:g.14955A>G , LRG_40:g.14955A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.645A>G	ENSP00000512095.1:n.645A>G
ENST00000489304.6:c.726A>G	ENSP00000512096.1:n.726A>G
ENST00000695670.1:n.612A>G
ENST00000695671.1:c.683A>G	ENSP00000512093.1:p.Tyr228Cys
ENST00000695674.1:n.1122A>G
ENST00000695675.1:n.2519A>G
ENST00000372285.8:c.643A>G MANE Select	ENSP00000361359.3:p.Ile215Val
ENST00000372276.7:c.581A>G	ENSP00000361350.3:p.Tyr194Cys
ENST00000372285.7:c.643A>G	ENSP00000361359.3:p.Ile215Val
ENST00000466205.5:c.545A>G
ENST00000477696.5:n.616A>G
ENST00000489304.5:n.719A>G
ENST00000620709.4:c.*190A>G	ENSP00000484074.1:n.*190A>G
NM_001250.5:c.643A>G	NP_001241.1:p.Ile215Val
NM_001302753.1:c.683A>G	NP_001289682.1:p.Tyr228Cys
NM_152854.3:c.581A>G	NP_690593.1:p.Tyr194Cys
NR_126502.1:n.736A>G
XM_005260617.2:c.643A>G	XP_005260674.1:p.Ile215Val
XM_005260619.2:c.487A>G	XP_005260676.1:p.Ile163Val
XR_936660.1:n.643A>G
NM_001322421.1:c.643A>G	NP_001309350.1:p.Ile215Val
NM_001322422.1:c.487A>G	NP_001309351.1:p.Ile163Val
NM_001362758.1:c.643A>G	NP_001349687.1:p.Ile215Val
NR_136327.1:n.639A>G
XM_005260619.3:c.487A>G	XP_005260676.1:p.Ile163Val
XM_017028135.1:c.683A>G	XP_016883624.1:p.Tyr228Cys
XM_017028136.1:c.581A>G	XP_016883625.1:p.Tyr194Cys
NM_001250.6:c.643A>G MANE Select	NP_001241.1:p.Ile215Val
NM_001302753.2:c.683A>G	NP_001289682.1:p.Tyr228Cys
NM_001322421.2:c.643A>G	NP_001309350.1:p.Ile215Val
NM_001322422.2:c.487A>G	NP_001309351.1:p.Ile163Val
NM_001362758.2:c.643A>G	NP_001349687.1:p.Ile215Val
NM_152854.4:c.581A>G	NP_690593.1:p.Tyr194Cys
NR_126502.2:n.676A>G
NR_136327.2:n.579A>G