Canonical Allele Identifier: CA315654851

Gene: CD40

Linked Data

• dbSNP Id: rs199980487
• MyVariant Identifiers: chr20:g.44757599C>T (hg19) ; chr20:g.46128960C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128960C>T , CM000682.2:g.46128960C>T	GRCh38
NC_000020.10:g.44757599C>T , CM000682.1:g.44757599C>T	GRCh37
NC_000020.9:g.44191006C>T	NCBI36
NG_007279.1:g.15694C>T , LRG_40:g.15694C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.756C>T	ENSP00000512095.1:n.756C>T
ENST00000489304.6:c.837C>T	ENSP00000512096.1:n.837C>T
ENST00000695675.1:n.2630C>T
ENST00000372285.8:c.754C>T MANE Select	ENSP00000361359.3:p.Gln252Ter
ENST00000372276.7:c.*80C>T	ENSP00000361350.3:n.*80C>T
ENST00000372285.7:c.754C>T	ENSP00000361359.3:p.Gln252Ter
ENST00000466205.5:c.656C>T
ENST00000477696.5:n.727C>T
ENST00000489304.5:n.830C>T
ENST00000620709.4:c.*301C>T	ENSP00000484074.1:n.*301C>T
NM_001250.5:c.754C>T	NP_001241.1:p.Gln252Ter
NM_001302753.1:c.*80C>T	NP_001289682.1:n.*80C>T
NM_152854.3:c.*80C>T	NP_690593.1:n.*80C>T
NR_126502.1:n.847C>T
XM_005260617.2:c.766C>T	XP_005260674.1:p.Gln256Ter
XM_005260619.2:c.610C>T	XP_005260676.1:p.Gln204Ter
XR_936660.1:n.754C>T
NM_001322421.1:c.766C>T	NP_001309350.1:p.Gln256Ter
NM_001322422.1:c.598C>T	NP_001309351.1:p.Gln200Ter
NM_001362758.1:c.*80C>T	NP_001349687.1:n.*80C>T
NR_136327.1:n.750C>T
XM_005260619.3:c.610C>T	XP_005260676.1:p.Gln204Ter
XM_017028135.1:c.789C>T	XP_016883624.1:p.Cys263=
XM_017028136.1:c.687C>T	XP_016883625.1:p.Cys229=
NM_001250.6:c.754C>T MANE Select	NP_001241.1:p.Gln252Ter
NM_001302753.2:c.*80C>T	NP_001289682.1:n.*80C>T
NM_001322421.2:c.766C>T	NP_001309350.1:p.Gln256Ter
NM_001322422.2:c.598C>T	NP_001309351.1:p.Gln200Ter
NM_001362758.2:c.*80C>T	NP_001349687.1:n.*80C>T
NM_152854.4:c.*80C>T	NP_690593.1:n.*80C>T
NR_126502.2:n.787C>T
NR_136327.2:n.690C>T