Canonical Allele Identifier: CA409209221

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44756825G>C (hg19) ; chr20:g.46128186G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128186G>C , CM000682.2:g.46128186G>C	GRCh38
NC_000020.10:g.44756825G>C , CM000682.1:g.44756825G>C	GRCh37
NC_000020.9:g.44190232G>C	NCBI36
NG_007279.1:g.14920G>C , LRG_40:g.14920G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.610G>C	ENSP00000512095.1:n.610G>C
ENST00000489304.6:c.691G>C	ENSP00000512096.1:n.691G>C
ENST00000695670.1:n.577G>C
ENST00000695671.1:c.648G>C	ENSP00000512093.1:p.Arg216=
ENST00000695674.1:n.1087G>C
ENST00000695675.1:n.2484G>C
ENST00000372285.8:c.608G>C MANE Select	ENSP00000361359.3:p.Gly203Ala
ENST00000372276.7:c.546G>C	ENSP00000361350.3:p.Arg182=
ENST00000372285.7:c.608G>C	ENSP00000361359.3:p.Gly203Ala
ENST00000466205.5:c.510G>C
ENST00000477696.5:n.581G>C
ENST00000489304.5:n.684G>C
ENST00000620709.4:c.*155G>C	ENSP00000484074.1:n.*155G>C
NM_001250.5:c.608G>C	NP_001241.1:p.Gly203Ala
NM_001302753.1:c.648G>C	NP_001289682.1:p.Arg216=
NM_152854.3:c.546G>C	NP_690593.1:p.Arg182=
NR_126502.1:n.701G>C
XM_005260617.2:c.608G>C	XP_005260674.1:p.Gly203Ala
XM_005260619.2:c.452G>C	XP_005260676.1:p.Gly151Ala
XR_936660.1:n.608G>C
NM_001322421.1:c.608G>C	NP_001309350.1:p.Gly203Ala
NM_001322422.1:c.452G>C	NP_001309351.1:p.Gly151Ala
NM_001362758.1:c.608G>C	NP_001349687.1:p.Gly203Ala
NR_136327.1:n.604G>C
XM_005260619.3:c.452G>C	XP_005260676.1:p.Gly151Ala
XM_017028135.1:c.648G>C	XP_016883624.1:p.Arg216=
XM_017028136.1:c.546G>C	XP_016883625.1:p.Arg182=
NM_001250.6:c.608G>C MANE Select	NP_001241.1:p.Gly203Ala
NM_001302753.2:c.648G>C	NP_001289682.1:p.Arg216=
NM_001322421.2:c.608G>C	NP_001309350.1:p.Gly203Ala
NM_001322422.2:c.452G>C	NP_001309351.1:p.Gly151Ala
NM_001362758.2:c.608G>C	NP_001349687.1:p.Gly203Ala
NM_152854.4:c.546G>C	NP_690593.1:p.Arg182=
NR_126502.2:n.641G>C
NR_136327.2:n.544G>C