Canonical Allele Identifier: CA409211552

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757534A>T (hg19) ; chr20:g.46128895A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128895A>T , CM000682.2:g.46128895A>T	GRCh38
NC_000020.10:g.44757534A>T , CM000682.1:g.44757534A>T	GRCh37
NC_000020.9:g.44190941A>T	NCBI36
NG_007279.1:g.15629A>T , LRG_40:g.15629A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.691A>T	ENSP00000512095.1:n.691A>T
ENST00000489304.6:c.772A>T	ENSP00000512096.1:n.772A>T
ENST00000695675.1:n.2565A>T
ENST00000372285.8:c.689A>T MANE Select	ENSP00000361359.3:p.Lys230Met
ENST00000372276.7:c.*15A>T	ENSP00000361350.3:n.*15A>T
ENST00000372285.7:c.689A>T	ENSP00000361359.3:p.Lys230Met
ENST00000466205.5:c.591A>T
ENST00000477696.5:n.662A>T
ENST00000489304.5:n.765A>T
ENST00000620709.4:c.*236A>T	ENSP00000484074.1:n.*236A>T
NM_001250.5:c.689A>T	NP_001241.1:p.Lys230Met
NM_001302753.1:c.*15A>T	NP_001289682.1:n.*15A>T
NM_152854.3:c.*15A>T	NP_690593.1:n.*15A>T
NR_126502.1:n.782A>T
XM_005260617.2:c.701A>T	XP_005260674.1:p.Lys234Met
XM_005260619.2:c.545A>T	XP_005260676.1:p.Lys182Met
XR_936660.1:n.689A>T
NM_001322421.1:c.701A>T	NP_001309350.1:p.Lys234Met
NM_001322422.1:c.533A>T	NP_001309351.1:p.Lys178Met
NM_001362758.1:c.*15A>T	NP_001349687.1:n.*15A>T
NR_136327.1:n.685A>T
XM_005260619.3:c.545A>T	XP_005260676.1:p.Lys182Met
XM_017028135.1:c.724A>T	XP_016883624.1:p.Ser242Cys
XM_017028136.1:c.622A>T	XP_016883625.1:p.Ser208Cys
NM_001250.6:c.689A>T MANE Select	NP_001241.1:p.Lys230Met
NM_001302753.2:c.*15A>T	NP_001289682.1:n.*15A>T
NM_001322421.2:c.701A>T	NP_001309350.1:p.Lys234Met
NM_001322422.2:c.533A>T	NP_001309351.1:p.Lys178Met
NM_001362758.2:c.*15A>T	NP_001349687.1:n.*15A>T
NM_152854.4:c.*15A>T	NP_690593.1:n.*15A>T
NR_126502.2:n.722A>T
NR_136327.2:n.625A>T