Canonical Allele Identifier: CA2653134247

Gene: CD40

Linked Data

• gnomAD v4: 20-46129232-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129232A>C , CM000682.2:g.46129232A>C	GRCh38
NC_000020.10:g.44757871A>C , CM000682.1:g.44757871A>C	GRCh37
NC_000020.9:g.44191278A>C	NCBI36
NG_007279.1:g.15966A>C , LRG_40:g.15966A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1109A>C	ENSP00000512096.1:n.1109A>C
ENST00000695675.1:n.2902A>C
ENST00000372285.8:c.*192A>C MANE Select	ENSP00000361359.3:n.*192A>C
ENST00000372276.7:c.*352A>C	ENSP00000361350.3:n.*352A>C
ENST00000372285.7:c.*192A>C	ENSP00000361359.3:n.*192A>C
ENST00000489304.5:n.1102A>C
ENST00000620709.4:c.*573A>C	ENSP00000484074.1:n.*573A>C
NM_001250.5:c.*192A>C	NP_001241.1:n.*192A>C
NM_001302753.1:c.*352A>C	NP_001289682.1:n.*352A>C
NM_152854.3:c.*352A>C	NP_690593.1:n.*352A>C
NR_126502.1:n.1119A>C
XM_005260617.2:c.*192A>C	XP_005260674.1:n.*192A>C
XM_005260619.2:c.*192A>C	XP_005260676.1:n.*192A>C
NM_001322421.1:c.*192A>C	NP_001309350.1:n.*192A>C
NM_001322422.1:c.*192A>C	NP_001309351.1:n.*192A>C
NM_001362758.1:c.*352A>C	NP_001349687.1:n.*352A>C
NR_136327.1:n.1022A>C
XM_005260619.3:c.*192A>C	XP_005260676.1:n.*192A>C
XM_017028135.1:c.*89A>C	XP_016883624.1:n.*89A>C
XM_017028136.1:c.*89A>C	XP_016883625.1:n.*89A>C
NM_001250.6:c.*192A>C MANE Select	NP_001241.1:n.*192A>C
NM_001302753.2:c.*352A>C	NP_001289682.1:n.*352A>C
NM_001322421.2:c.*192A>C	NP_001309350.1:n.*192A>C
NM_001322422.2:c.*192A>C	NP_001309351.1:n.*192A>C
NM_001362758.2:c.*352A>C	NP_001349687.1:n.*352A>C
NM_152854.4:c.*352A>C	NP_690593.1:n.*352A>C
NR_126502.2:n.1059A>C
NR_136327.2:n.962A>C