Canonical Allele Identifier: CA2653134199

Gene: CD40

Linked Data

• gnomAD v4: 20-46129209-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129209G>A , CM000682.2:g.46129209G>A	GRCh38
NC_000020.10:g.44757848G>A , CM000682.1:g.44757848G>A	GRCh37
NC_000020.9:g.44191255G>A	NCBI36
NG_007279.1:g.15943G>A , LRG_40:g.15943G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1086G>A	ENSP00000512096.1:n.1086G>A
ENST00000695675.1:n.2879G>A
ENST00000372285.8:c.*169G>A MANE Select	ENSP00000361359.3:n.*169G>A
ENST00000372276.7:c.*329G>A	ENSP00000361350.3:n.*329G>A
ENST00000372285.7:c.*169G>A	ENSP00000361359.3:n.*169G>A
ENST00000489304.5:n.1079G>A
ENST00000620709.4:c.*550G>A	ENSP00000484074.1:n.*550G>A
NM_001250.5:c.*169G>A	NP_001241.1:n.*169G>A
NM_001302753.1:c.*329G>A	NP_001289682.1:n.*329G>A
NM_152854.3:c.*329G>A	NP_690593.1:n.*329G>A
NR_126502.1:n.1096G>A
XM_005260617.2:c.*169G>A	XP_005260674.1:n.*169G>A
XM_005260619.2:c.*169G>A	XP_005260676.1:n.*169G>A
NM_001322421.1:c.*169G>A	NP_001309350.1:n.*169G>A
NM_001322422.1:c.*169G>A	NP_001309351.1:n.*169G>A
NM_001362758.1:c.*329G>A	NP_001349687.1:n.*329G>A
NR_136327.1:n.999G>A
XM_005260619.3:c.*169G>A	XP_005260676.1:n.*169G>A
XM_017028135.1:c.*66G>A	XP_016883624.1:n.*66G>A
XM_017028136.1:c.*66G>A	XP_016883625.1:n.*66G>A
NM_001250.6:c.*169G>A MANE Select	NP_001241.1:n.*169G>A
NM_001302753.2:c.*329G>A	NP_001289682.1:n.*329G>A
NM_001322421.2:c.*169G>A	NP_001309350.1:n.*169G>A
NM_001322422.2:c.*169G>A	NP_001309351.1:n.*169G>A
NM_001362758.2:c.*329G>A	NP_001349687.1:n.*329G>A
NM_152854.4:c.*329G>A	NP_690593.1:n.*329G>A
NR_126502.2:n.1036G>A
NR_136327.2:n.939G>A