Canonical Allele Identifier: CA657647826

Gene: CD40

Linked Data

• COSMIC: COSN24307091 ; COSN24307092

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129156_46129157insG , CM000682.2:g.46129156_46129157insG	GRCh38
NC_000020.10:g.44757795_44757796insG , CM000682.1:g.44757795_44757796insG	GRCh37
NC_000020.9:g.44191202_44191203insG	NCBI36
NG_007279.1:g.15890_15891insG , LRG_40:g.15890_15891insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1033_1034insG	ENSP00000512096.1:n.1033_1034insG
ENST00000695675.1:n.2826_2827insG
ENST00000372285.8:c.*116_*117insG MANE Select	ENSP00000361359.3:n.*116_*117insG
ENST00000372276.7:c.*276_*277insG	ENSP00000361350.3:n.*276_*277insG
ENST00000372285.7:c.*116_*117insG	ENSP00000361359.3:n.*116_*117insG
ENST00000489304.5:n.1026_1027insG
ENST00000620709.4:c.*497_*498insG	ENSP00000484074.1:n.*497_*498insG
NM_001250.5:c.*116_*117insG	NP_001241.1:n.*116_*117insG
NM_001302753.1:c.*276_*277insG	NP_001289682.1:n.*276_*277insG
NM_152854.3:c.*276_*277insG	NP_690593.1:n.*276_*277insG
NR_126502.1:n.1043_1044insG
XM_005260617.2:c.*116_*117insG	XP_005260674.1:n.*116_*117insG
XM_005260619.2:c.*116_*117insG	XP_005260676.1:n.*116_*117insG
NM_001322421.1:c.*116_*117insG	NP_001309350.1:n.*116_*117insG
NM_001322422.1:c.*116_*117insG	NP_001309351.1:n.*116_*117insG
NM_001362758.1:c.*276_*277insG	NP_001349687.1:n.*276_*277insG
NR_136327.1:n.946_947insG
XM_005260619.3:c.*116_*117insG	XP_005260676.1:n.*116_*117insG
XM_017028135.1:c.*13_*14insG	XP_016883624.1:n.*13_*14insG
XM_017028136.1:c.*13_*14insG	XP_016883625.1:n.*13_*14insG
NM_001250.6:c.*116_*117insG MANE Select	NP_001241.1:n.*116_*117insG
NM_001302753.2:c.*276_*277insG	NP_001289682.1:n.*276_*277insG
NM_001322421.2:c.*116_*117insG	NP_001309350.1:n.*116_*117insG
NM_001322422.2:c.*116_*117insG	NP_001309351.1:n.*116_*117insG
NM_001362758.2:c.*276_*277insG	NP_001349687.1:n.*276_*277insG
NM_152854.4:c.*276_*277insG	NP_690593.1:n.*276_*277insG
NR_126502.2:n.983_984insG
NR_136327.2:n.886_887insG