Canonical Allele Identifier: CA409212464

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757672G>C (hg19) ; chr20:g.46129033G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129033G>C , CM000682.2:g.46129033G>C	GRCh38
NC_000020.10:g.44757672G>C , CM000682.1:g.44757672G>C	GRCh37
NC_000020.9:g.44191079G>C	NCBI36
NG_007279.1:g.15767G>C , LRG_40:g.15767G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.910G>C	ENSP00000512096.1:n.910G>C
ENST00000695675.1:n.2703G>C
ENST00000372285.8:c.827G>C MANE Select	ENSP00000361359.3:p.Arg276Thr
ENST00000372276.7:c.*153G>C	ENSP00000361350.3:n.*153G>C
ENST00000372285.7:c.827G>C	ENSP00000361359.3:p.Arg276Thr
ENST00000466205.5:c.729G>C
ENST00000489304.5:n.903G>C
ENST00000620709.4:c.*374G>C	ENSP00000484074.1:n.*374G>C
NM_001250.5:c.827G>C	NP_001241.1:p.Arg276Thr
NM_001302753.1:c.*153G>C	NP_001289682.1:n.*153G>C
NM_152854.3:c.*153G>C	NP_690593.1:n.*153G>C
NR_126502.1:n.920G>C
XM_005260617.2:c.839G>C	XP_005260674.1:p.Arg280Thr
XM_005260619.2:c.683G>C	XP_005260676.1:p.Arg228Thr
XR_936660.1:n.827G>C
NM_001322421.1:c.839G>C	NP_001309350.1:p.Arg280Thr
NM_001322422.1:c.671G>C	NP_001309351.1:p.Arg224Thr
NM_001362758.1:c.*153G>C	NP_001349687.1:n.*153G>C
NR_136327.1:n.823G>C
XM_005260619.3:c.683G>C	XP_005260676.1:p.Arg228Thr
XM_017028135.1:c.862G>C	XP_016883624.1:p.Asp288His
XM_017028136.1:c.760G>C	XP_016883625.1:p.Asp254His
NM_001250.6:c.827G>C MANE Select	NP_001241.1:p.Arg276Thr
NM_001302753.2:c.*153G>C	NP_001289682.1:n.*153G>C
NM_001322421.2:c.839G>C	NP_001309350.1:p.Arg280Thr
NM_001322422.2:c.671G>C	NP_001309351.1:p.Arg224Thr
NM_001362758.2:c.*153G>C	NP_001349687.1:n.*153G>C
NM_152854.4:c.*153G>C	NP_690593.1:n.*153G>C
NR_126502.2:n.860G>C
NR_136327.2:n.763G>C