Canonical Allele Identifier: CA409211539

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757533A>C (hg19) ; chr20:g.46128894A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128894A>C , CM000682.2:g.46128894A>C	GRCh38
NC_000020.10:g.44757533A>C , CM000682.1:g.44757533A>C	GRCh37
NC_000020.9:g.44190940A>C	NCBI36
NG_007279.1:g.15628A>C , LRG_40:g.15628A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.690A>C	ENSP00000512095.1:n.690A>C
ENST00000489304.6:c.771A>C	ENSP00000512096.1:n.771A>C
ENST00000695675.1:n.2564A>C
ENST00000372285.8:c.688A>C MANE Select	ENSP00000361359.3:p.Lys230Gln
ENST00000372276.7:c.*14A>C	ENSP00000361350.3:n.*14A>C
ENST00000372285.7:c.688A>C	ENSP00000361359.3:p.Lys230Gln
ENST00000466205.5:c.590A>C
ENST00000477696.5:n.661A>C
ENST00000489304.5:n.764A>C
ENST00000620709.4:c.*235A>C	ENSP00000484074.1:n.*235A>C
NM_001250.5:c.688A>C	NP_001241.1:p.Lys230Gln
NM_001302753.1:c.*14A>C	NP_001289682.1:n.*14A>C
NM_152854.3:c.*14A>C	NP_690593.1:n.*14A>C
NR_126502.1:n.781A>C
XM_005260617.2:c.700A>C	XP_005260674.1:p.Lys234Gln
XM_005260619.2:c.544A>C	XP_005260676.1:p.Lys182Gln
XR_936660.1:n.688A>C
NM_001322421.1:c.700A>C	NP_001309350.1:p.Lys234Gln
NM_001322422.1:c.532A>C	NP_001309351.1:p.Lys178Gln
NM_001362758.1:c.*14A>C	NP_001349687.1:n.*14A>C
NR_136327.1:n.684A>C
XM_005260619.3:c.544A>C	XP_005260676.1:p.Lys182Gln
XM_017028135.1:c.723A>C	XP_016883624.1:p.Pro241=
XM_017028136.1:c.621A>C	XP_016883625.1:p.Pro207=
NM_001250.6:c.688A>C MANE Select	NP_001241.1:p.Lys230Gln
NM_001302753.2:c.*14A>C	NP_001289682.1:n.*14A>C
NM_001322421.2:c.700A>C	NP_001309350.1:p.Lys234Gln
NM_001322422.2:c.532A>C	NP_001309351.1:p.Lys178Gln
NM_001362758.2:c.*14A>C	NP_001349687.1:n.*14A>C
NM_152854.4:c.*14A>C	NP_690593.1:n.*14A>C
NR_126502.2:n.721A>C
NR_136327.2:n.624A>C