Canonical Allele Identifier: CA657647822

Gene: CD40

Linked Data

• COSMIC: COSN19655627

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129047_46129048insG , CM000682.2:g.46129047_46129048insG	GRCh38
NC_000020.10:g.44757686_44757687insG , CM000682.1:g.44757686_44757687insG	GRCh37
NC_000020.9:g.44191093_44191094insG	NCBI36
NG_007279.1:g.15781_15782insG , LRG_40:g.15781_15782insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.924_925insG	ENSP00000512096.1:n.924_925insG
ENST00000695675.1:n.2717_2718insG
ENST00000372285.8:c.*7_*8insG MANE Select	ENSP00000361359.3:n.*7_*8insG
ENST00000372276.7:c.*167_*168insG	ENSP00000361350.3:n.*167_*168insG
ENST00000372285.7:c.*7_*8insG	ENSP00000361359.3:n.*7_*8insG
ENST00000466205.5:c.743_744insG
ENST00000489304.5:n.917_918insG
ENST00000620709.4:c.*388_*389insG	ENSP00000484074.1:n.*388_*389insG
NM_001250.5:c.*7_*8insG	NP_001241.1:n.*7_*8insG
NM_001302753.1:c.*167_*168insG	NP_001289682.1:n.*167_*168insG
NM_152854.3:c.*167_*168insG	NP_690593.1:n.*167_*168insG
NR_126502.1:n.934_935insG
XM_005260617.2:c.*7_*8insG	XP_005260674.1:n.*7_*8insG
XM_005260619.2:c.*7_*8insG	XP_005260676.1:n.*7_*8insG
XR_936660.1:n.841_842insG
NM_001322421.1:c.*7_*8insG	NP_001309350.1:n.*7_*8insG
NM_001322422.1:c.*7_*8insG	NP_001309351.1:n.*7_*8insG
NM_001362758.1:c.*167_*168insG	NP_001349687.1:n.*167_*168insG
NR_136327.1:n.837_838insG
XM_005260619.3:c.*7_*8insG	XP_005260676.1:n.*7_*8insG
XM_017028135.1:c.876_877insG	XP_016883624.1:p.Pro293AlafsTer?
XM_017028136.1:c.774_775insG	XP_016883625.1:p.Pro259AlafsTer?
NM_001250.6:c.*7_*8insG MANE Select	NP_001241.1:n.*7_*8insG
NM_001302753.2:c.*167_*168insG	NP_001289682.1:n.*167_*168insG
NM_001322421.2:c.*7_*8insG	NP_001309350.1:n.*7_*8insG
NM_001322422.2:c.*7_*8insG	NP_001309351.1:n.*7_*8insG
NM_001362758.2:c.*167_*168insG	NP_001349687.1:n.*167_*168insG
NM_152854.4:c.*167_*168insG	NP_690593.1:n.*167_*168insG
NR_126502.2:n.874_875insG
NR_136327.2:n.777_778insG