Canonical Allele Identifier: CA510657745

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757526C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128887C>A , CM000682.2:g.46128887C>A	GRCh38
NC_000020.10:g.44757526C>A , CM000682.1:g.44757526C>A	GRCh37
NC_000020.9:g.44190933C>A	NCBI36
NG_007279.1:g.15621C>A , LRG_40:g.15621C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.683C>A	ENSP00000512095.1:n.683C>A
ENST00000489304.6:c.764C>A	ENSP00000512096.1:n.764C>A
ENST00000695675.1:n.2557C>A
ENST00000372285.8:c.681C>A MANE Select	ENSP00000361359.3:p.Pro227=
ENST00000372276.7:c.*7C>A	ENSP00000361350.3:n.*7C>A
ENST00000372285.7:c.681C>A	ENSP00000361359.3:p.Pro227=
ENST00000466205.5:c.583C>A
ENST00000477696.5:n.654C>A
ENST00000489304.5:n.757C>A
ENST00000620709.4:c.*228C>A	ENSP00000484074.1:n.*228C>A
NM_001250.5:c.681C>A	NP_001241.1:p.Pro227=
NM_001302753.1:c.*7C>A	NP_001289682.1:n.*7C>A
NM_152854.3:c.*7C>A	NP_690593.1:n.*7C>A
NR_126502.1:n.774C>A
XM_005260617.2:c.693C>A	XP_005260674.1:p.Pro231=
XM_005260619.2:c.537C>A	XP_005260676.1:p.Pro179=
XR_936660.1:n.681C>A
NM_001322421.1:c.693C>A	NP_001309350.1:p.Pro231=
NM_001322422.1:c.525C>A	NP_001309351.1:p.Pro175=
NM_001362758.1:c.*7C>A	NP_001349687.1:n.*7C>A
NR_136327.1:n.677C>A
XM_005260619.3:c.537C>A	XP_005260676.1:p.Pro179=
XM_017028135.1:c.716C>A	XP_016883624.1:p.Pro239His
XM_017028136.1:c.614C>A	XP_016883625.1:p.Pro205His
NM_001250.6:c.681C>A MANE Select	NP_001241.1:p.Pro227=
NM_001302753.2:c.*7C>A	NP_001289682.1:n.*7C>A
NM_001322421.2:c.693C>A	NP_001309350.1:p.Pro231=
NM_001322422.2:c.525C>A	NP_001309351.1:p.Pro175=
NM_001362758.2:c.*7C>A	NP_001349687.1:n.*7C>A
NM_152854.4:c.*7C>A	NP_690593.1:n.*7C>A
NR_126502.2:n.714C>A
NR_136327.2:n.617C>A