Canonical Allele Identifier: CA2366530726

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46122590_46122594delinsTCCTG , CM000682.2:g.46122590_46122594delinsTCCTG	GRCh38
NC_000020.10:g.44751229_44751233delinsTCCTG , CM000682.1:g.44751229_44751233delinsTCCTG	GRCh37
NC_000020.9:g.44184636_44184640delinsTCCTG	NCBI36
NG_007279.1:g.9324_9328delinsTCCTG , LRG_40:g.9324_9328delinsTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.353-20_353-16delinsTCCTG	ENSP00000512095.1:n.353-20_353-16delinsTCCTG
ENST00000489304.6:c.257-20_257-16delinsTCCTG	ENSP00000512096.1:n.257-20_257-16delinsTCCTG
ENST00000695669.1:n.330-20_330-16delinsTCCTG
ENST00000695670.1:n.237-20_237-16delinsTCCTG
ENST00000695671.1:c.257-20_257-16delinsTCCTG	ENSP00000512093.1:n.257-20_257-16delinsTCCTG
ENST00000695672.1:n.182-20_182-16delinsTCCTG
ENST00000695673.1:n.122-20_122-16delinsTCCTG
ENST00000372285.8:c.257-20_257-16delinsTCCTG MANE Select	ENSP00000361359.3:n.257-20_257-16delinsTCCTG
ENST00000372276.7:c.257-20_257-16delinsTCCTG	ENSP00000361350.3:n.257-20_257-16delinsTCCTG
ENST00000372285.7:c.257-20_257-16delinsTCCTG	ENSP00000361359.3:n.257-20_257-16delinsTCCTG
ENST00000461171.1:n.42-20_42-16delinsTCCTG
ENST00000466205.5:c.253-20_253-16delinsTCCTG
ENST00000477696.5:n.324-20_324-16delinsTCCTG
ENST00000489304.5:n.250-20_250-16delinsTCCTG
ENST00000620709.4:c.257-20_257-16delinsTCCTG	ENSP00000484074.1:n.257-20_257-16delinsTCCTG
NM_001250.5:c.257-20_257-16delinsTCCTG	NP_001241.1:n.257-20_257-16delinsTCCTG
NM_001302753.1:c.257-20_257-16delinsTCCTG	NP_001289682.1:n.257-20_257-16delinsTCCTG
NM_152854.3:c.257-20_257-16delinsTCCTG	NP_690593.1:n.257-20_257-16delinsTCCTG
NR_126502.1:n.347-20_347-16delinsTCCTG
XM_005260617.2:c.257-20_257-16delinsTCCTG	XP_005260674.1:n.257-20_257-16delinsTCCTG
XM_005260619.2:c.257-20_257-16delinsTCCTG	XP_005260676.1:n.257-20_257-16delinsTCCTG
XM_011529109.1:c.257-20_257-16delinsTCCTG	XP_011527411.1:n.257-20_257-16delinsTCCTG
XR_936660.1:n.351-20_351-16delinsTCCTG
NM_001322421.1:c.257-20_257-16delinsTCCTG	NP_001309350.1:n.257-20_257-16delinsTCCTG
NM_001322422.1:c.257-20_257-16delinsTCCTG	NP_001309351.1:n.257-20_257-16delinsTCCTG
NM_001362758.1:c.257-20_257-16delinsTCCTG	NP_001349687.1:n.257-20_257-16delinsTCCTG
NR_136327.1:n.347-20_347-16delinsTCCTG
XM_005260619.3:c.257-20_257-16delinsTCCTG	XP_005260676.1:n.257-20_257-16delinsTCCTG
XM_011529109.2:c.257-20_257-16delinsTCCTG	XP_011527411.1:n.257-20_257-16delinsTCCTG
XM_017028135.1:c.257-20_257-16delinsTCCTG	XP_016883624.1:n.257-20_257-16delinsTCCTG
XM_017028136.1:c.257-20_257-16delinsTCCTG	XP_016883625.1:n.257-20_257-16delinsTCCTG
NM_001250.6:c.257-20_257-16delinsTCCTG MANE Select	NP_001241.1:n.257-20_257-16delinsTCCTG
NM_001302753.2:c.257-20_257-16delinsTCCTG	NP_001289682.1:n.257-20_257-16delinsTCCTG
NM_001322421.2:c.257-20_257-16delinsTCCTG	NP_001309350.1:n.257-20_257-16delinsTCCTG
NM_001322422.2:c.257-20_257-16delinsTCCTG	NP_001309351.1:n.257-20_257-16delinsTCCTG
NM_001362758.2:c.257-20_257-16delinsTCCTG	NP_001349687.1:n.257-20_257-16delinsTCCTG
NM_152854.4:c.257-20_257-16delinsTCCTG	NP_690593.1:n.257-20_257-16delinsTCCTG
NR_126502.2:n.287-20_287-16delinsTCCTG
NR_136327.2:n.287-20_287-16delinsTCCTG