Canonical Allele Identifier: CA2577415088

Gene: CD40

Linked Data

• gnomAD v4: 20-46128796-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128796G>T , CM000682.2:g.46128796G>T	GRCh38
NC_000020.10:g.44757435G>T , CM000682.1:g.44757435G>T	GRCh37
NC_000020.9:g.44190842G>T	NCBI36
NG_007279.1:g.15530G>T , LRG_40:g.15530G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.678-86G>T	ENSP00000512095.1:n.678-86G>T
ENST00000489304.6:c.759-86G>T	ENSP00000512096.1:n.759-86G>T
ENST00000695675.1:n.2552-86G>T
ENST00000372285.8:c.676-86G>T MANE Select	ENSP00000361359.3:n.676-86G>T
ENST00000372276.7:c.*2-86G>T	ENSP00000361350.3:n.*2-86G>T
ENST00000372285.7:c.676-86G>T	ENSP00000361359.3:n.676-86G>T
ENST00000466205.5:c.578-86G>T
ENST00000477696.5:n.649-86G>T
ENST00000489304.5:n.752-86G>T
ENST00000620709.4:c.*223-86G>T	ENSP00000484074.1:n.*223-86G>T
NM_001250.5:c.676-86G>T	NP_001241.1:n.676-86G>T
NM_001302753.1:c.*2-86G>T	NP_001289682.1:n.*2-86G>T
NM_152854.3:c.*2-86G>T	NP_690593.1:n.*2-86G>T
NR_126502.1:n.769-86G>T
XM_005260617.2:c.688-86G>T	XP_005260674.1:n.688-86G>T
XM_005260619.2:c.532-86G>T	XP_005260676.1:n.532-86G>T
XR_936660.1:n.676-86G>T
NM_001322421.1:c.688-86G>T	NP_001309350.1:n.688-86G>T
NM_001322422.1:c.520-86G>T	NP_001309351.1:n.520-86G>T
NM_001362758.1:c.*2-86G>T	NP_001349687.1:n.*2-86G>T
NR_136327.1:n.672-86G>T
XM_005260619.3:c.532-86G>T	XP_005260676.1:n.532-86G>T
XM_017028135.1:c.711-86G>T	XP_016883624.1:n.711-86G>T
XM_017028136.1:c.609-86G>T	XP_016883625.1:n.609-86G>T
NM_001250.6:c.676-86G>T MANE Select	NP_001241.1:n.676-86G>T
NM_001302753.2:c.*2-86G>T	NP_001289682.1:n.*2-86G>T
NM_001322421.2:c.688-86G>T	NP_001309350.1:n.688-86G>T
NM_001322422.2:c.520-86G>T	NP_001309351.1:n.520-86G>T
NM_001362758.2:c.*2-86G>T	NP_001349687.1:n.*2-86G>T
NM_152854.4:c.*2-86G>T	NP_690593.1:n.*2-86G>T
NR_126502.2:n.709-86G>T
NR_136327.2:n.612-86G>T