Canonical Allele Identifier: CA409212325

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757656A>G (hg19) ; chr20:g.46129017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129017A>G , CM000682.2:g.46129017A>G	GRCh38
NC_000020.10:g.44757656A>G , CM000682.1:g.44757656A>G	GRCh37
NC_000020.9:g.44191063A>G	NCBI36
NG_007279.1:g.15751A>G , LRG_40:g.15751A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.894A>G	ENSP00000512096.1:n.894A>G
ENST00000695675.1:n.2687A>G
ENST00000372285.8:c.811A>G MANE Select	ENSP00000361359.3:p.Ile271Val
ENST00000372276.7:c.*137A>G	ENSP00000361350.3:n.*137A>G
ENST00000372285.7:c.811A>G	ENSP00000361359.3:p.Ile271Val
ENST00000466205.5:c.713A>G
ENST00000489304.5:n.887A>G
ENST00000620709.4:c.*358A>G	ENSP00000484074.1:n.*358A>G
NM_001250.5:c.811A>G	NP_001241.1:p.Ile271Val
NM_001302753.1:c.*137A>G	NP_001289682.1:n.*137A>G
NM_152854.3:c.*137A>G	NP_690593.1:n.*137A>G
NR_126502.1:n.904A>G
XM_005260617.2:c.823A>G	XP_005260674.1:p.Ile275Val
XM_005260619.2:c.667A>G	XP_005260676.1:p.Ile223Val
XR_936660.1:n.811A>G
NM_001322421.1:c.823A>G	NP_001309350.1:p.Ile275Val
NM_001322422.1:c.655A>G	NP_001309351.1:p.Ile219Val
NM_001362758.1:c.*137A>G	NP_001349687.1:n.*137A>G
NR_136327.1:n.807A>G
XM_005260619.3:c.667A>G	XP_005260676.1:p.Ile223Val
XM_017028135.1:c.846A>G	XP_016883624.1:p.Ala282=
XM_017028136.1:c.744A>G	XP_016883625.1:p.Ala248=
NM_001250.6:c.811A>G MANE Select	NP_001241.1:p.Ile271Val
NM_001302753.2:c.*137A>G	NP_001289682.1:n.*137A>G
NM_001322421.2:c.823A>G	NP_001309350.1:p.Ile275Val
NM_001322422.2:c.655A>G	NP_001309351.1:p.Ile219Val
NM_001362758.2:c.*137A>G	NP_001349687.1:n.*137A>G
NM_152854.4:c.*137A>G	NP_690593.1:n.*137A>G
NR_126502.2:n.844A>G
NR_136327.2:n.747A>G