Canonical Allele Identifier: CA409211519

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757530C>T (hg19) ; chr20:g.46128891C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128891C>T , CM000682.2:g.46128891C>T	GRCh38
NC_000020.10:g.44757530C>T , CM000682.1:g.44757530C>T	GRCh37
NC_000020.9:g.44190937C>T	NCBI36
NG_007279.1:g.15625C>T , LRG_40:g.15625C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.687C>T	ENSP00000512095.1:n.687C>T
ENST00000489304.6:c.768C>T	ENSP00000512096.1:n.768C>T
ENST00000695675.1:n.2561C>T
ENST00000372285.8:c.685C>T MANE Select	ENSP00000361359.3:p.Pro229Ser
ENST00000372276.7:c.*11C>T	ENSP00000361350.3:n.*11C>T
ENST00000372285.7:c.685C>T	ENSP00000361359.3:p.Pro229Ser
ENST00000466205.5:c.587C>T
ENST00000477696.5:n.658C>T
ENST00000489304.5:n.761C>T
ENST00000620709.4:c.*232C>T	ENSP00000484074.1:n.*232C>T
NM_001250.5:c.685C>T	NP_001241.1:p.Pro229Ser
NM_001302753.1:c.*11C>T	NP_001289682.1:n.*11C>T
NM_152854.3:c.*11C>T	NP_690593.1:n.*11C>T
NR_126502.1:n.778C>T
XM_005260617.2:c.697C>T	XP_005260674.1:p.Pro233Ser
XM_005260619.2:c.541C>T	XP_005260676.1:p.Pro181Ser
XR_936660.1:n.685C>T
NM_001322421.1:c.697C>T	NP_001309350.1:p.Pro233Ser
NM_001322422.1:c.529C>T	NP_001309351.1:p.Pro177Ser
NM_001362758.1:c.*11C>T	NP_001349687.1:n.*11C>T
NR_136327.1:n.681C>T
XM_005260619.3:c.541C>T	XP_005260676.1:p.Pro181Ser
XM_017028135.1:c.720C>T	XP_016883624.1:p.Thr240=
XM_017028136.1:c.618C>T	XP_016883625.1:p.Thr206=
NM_001250.6:c.685C>T MANE Select	NP_001241.1:p.Pro229Ser
NM_001302753.2:c.*11C>T	NP_001289682.1:n.*11C>T
NM_001322421.2:c.697C>T	NP_001309350.1:p.Pro233Ser
NM_001322422.2:c.529C>T	NP_001309351.1:p.Pro177Ser
NM_001362758.2:c.*11C>T	NP_001349687.1:n.*11C>T
NM_152854.4:c.*11C>T	NP_690593.1:n.*11C>T
NR_126502.2:n.718C>T
NR_136327.2:n.621C>T