Canonical Allele Identifier: CA2653133795

Gene: CD40

Linked Data

• gnomAD v4: 20-46128793-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128797del , CM000682.2:g.46128797del	GRCh38
NC_000020.10:g.44757436del , CM000682.1:g.44757436del	GRCh37
NC_000020.9:g.44190843del	NCBI36
NG_007279.1:g.15531del , LRG_40:g.15531del

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.678-85del	ENSP00000512095.1:n.678-85del
ENST00000489304.6:c.759-85del	ENSP00000512096.1:n.759-85del
ENST00000695675.1:n.2552-85del
ENST00000372285.8:c.676-85del MANE Select	ENSP00000361359.3:n.676-85del
ENST00000372276.7:c.*2-85del	ENSP00000361350.3:n.*2-85del
ENST00000372285.7:c.676-85del	ENSP00000361359.3:n.676-85del
ENST00000466205.5:c.578-85del
ENST00000477696.5:n.649-85del
ENST00000489304.5:n.752-85del
ENST00000620709.4:c.*223-85del	ENSP00000484074.1:n.*223-85del
NM_001250.5:c.676-85del	NP_001241.1:n.676-85del
NM_001302753.1:c.*2-85del	NP_001289682.1:n.*2-85del
NM_152854.3:c.*2-85del	NP_690593.1:n.*2-85del
NR_126502.1:n.769-85del
XM_005260617.2:c.688-85del	XP_005260674.1:n.688-85del
XM_005260619.2:c.532-85del	XP_005260676.1:n.532-85del
XR_936660.1:n.676-85del
NM_001322421.1:c.688-85del	NP_001309350.1:n.688-85del
NM_001322422.1:c.520-85del	NP_001309351.1:n.520-85del
NM_001362758.1:c.*2-85del	NP_001349687.1:n.*2-85del
NR_136327.1:n.672-85del
XM_005260619.3:c.532-85del	XP_005260676.1:n.532-85del
XM_017028135.1:c.711-85del	XP_016883624.1:n.711-85del
XM_017028136.1:c.609-85del	XP_016883625.1:n.609-85del
NM_001250.6:c.676-85del MANE Select	NP_001241.1:n.676-85del
NM_001302753.2:c.*2-85del	NP_001289682.1:n.*2-85del
NM_001322421.2:c.688-85del	NP_001309350.1:n.688-85del
NM_001322422.2:c.520-85del	NP_001309351.1:n.520-85del
NM_001362758.2:c.*2-85del	NP_001349687.1:n.*2-85del
NM_152854.4:c.*2-85del	NP_690593.1:n.*2-85del
NR_126502.2:n.709-85del
NR_136327.2:n.612-85del