Canonical Allele Identifier: CA409211663

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757551A>T (hg19) ; chr20:g.46128912A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128912A>T , CM000682.2:g.46128912A>T	GRCh38
NC_000020.10:g.44757551A>T , CM000682.1:g.44757551A>T	GRCh37
NC_000020.9:g.44190958A>T	NCBI36
NG_007279.1:g.15646A>T , LRG_40:g.15646A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.708A>T	ENSP00000512095.1:n.708A>T
ENST00000489304.6:c.789A>T	ENSP00000512096.1:n.789A>T
ENST00000695675.1:n.2582A>T
ENST00000372285.8:c.706A>T MANE Select	ENSP00000361359.3:p.Ile236Phe
ENST00000372276.7:c.*32A>T	ENSP00000361350.3:n.*32A>T
ENST00000372285.7:c.706A>T	ENSP00000361359.3:p.Ile236Phe
ENST00000466205.5:c.608A>T
ENST00000477696.5:n.679A>T
ENST00000489304.5:n.782A>T
ENST00000620709.4:c.*253A>T	ENSP00000484074.1:n.*253A>T
NM_001250.5:c.706A>T	NP_001241.1:p.Ile236Phe
NM_001302753.1:c.*32A>T	NP_001289682.1:n.*32A>T
NM_152854.3:c.*32A>T	NP_690593.1:n.*32A>T
NR_126502.1:n.799A>T
XM_005260617.2:c.718A>T	XP_005260674.1:p.Ile240Phe
XM_005260619.2:c.562A>T	XP_005260676.1:p.Ile188Phe
XR_936660.1:n.706A>T
NM_001322421.1:c.718A>T	NP_001309350.1:p.Ile240Phe
NM_001322422.1:c.550A>T	NP_001309351.1:p.Ile184Phe
NM_001362758.1:c.*32A>T	NP_001349687.1:n.*32A>T
NR_136327.1:n.702A>T
XM_005260619.3:c.562A>T	XP_005260676.1:p.Ile188Phe
XM_017028135.1:c.741A>T	XP_016883624.1:p.Arg247Ser
XM_017028136.1:c.639A>T	XP_016883625.1:p.Arg213Ser
NM_001250.6:c.706A>T MANE Select	NP_001241.1:p.Ile236Phe
NM_001302753.2:c.*32A>T	NP_001289682.1:n.*32A>T
NM_001322421.2:c.718A>T	NP_001309350.1:p.Ile240Phe
NM_001322422.2:c.550A>T	NP_001309351.1:p.Ile184Phe
NM_001362758.2:c.*32A>T	NP_001349687.1:n.*32A>T
NM_152854.4:c.*32A>T	NP_690593.1:n.*32A>T
NR_126502.2:n.739A>T
NR_136327.2:n.642A>T