Canonical Allele Identifier: CA2840601113

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46118336_46118337del , CM000682.2:g.46118336_46118337del	GRCh38
NC_000020.10:g.44746975_44746976del , CM000682.1:g.44746975_44746976del	GRCh37
NC_000020.9:g.44180382_44180383del	NCBI36
NG_007279.1:g.5070_5071del , LRG_40:g.5070_5071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695669.1:n.66_67del
ENST00000695670.1:n.52_53del
ENST00000695671.1:c.-8_-7del	ENSP00000512093.1:n.-8_-7del
ENST00000372285.8:c.-8_-7del MANE Select	ENSP00000361359.3:n.-8_-7del
ENST00000372276.7:c.-8_-7del	ENSP00000361350.3:n.-8_-7del
ENST00000372285.7:c.-8_-7del	ENSP00000361359.3:n.-8_-7del
ENST00000620709.4:c.-8_-7del	ENSP00000484074.1:n.-8_-7del
NM_001250.5:c.-8_-7del	NP_001241.1:n.-8_-7del
NM_001302753.1:c.-8_-7del	NP_001289682.1:n.-8_-7del
NM_152854.3:c.-8_-7del	NP_690593.1:n.-8_-7del
NR_126502.1:n.83_84del
XM_005260617.2:c.-8_-7del	XP_005260674.1:n.-8_-7del
XM_005260619.2:c.-8_-7del	XP_005260676.1:n.-8_-7del
XM_011529109.1:c.-8_-7del	XP_011527411.1:n.-8_-7del
XR_936660.1:n.87_88del
NM_001322421.1:c.-8_-7del	NP_001309350.1:n.-8_-7del
NM_001322422.1:c.-8_-7del	NP_001309351.1:n.-8_-7del
NM_001362758.1:c.-8_-7del	NP_001349687.1:n.-8_-7del
NR_136327.1:n.83_84del
XM_005260619.3:c.-8_-7del	XP_005260676.1:n.-8_-7del
XM_011529109.2:c.-8_-7del	XP_011527411.1:n.-8_-7del
XM_017028135.1:c.-8_-7del	XP_016883624.1:n.-8_-7del
XM_017028136.1:c.-8_-7del	XP_016883625.1:n.-8_-7del
NM_001250.6:c.-8_-7del MANE Select	NP_001241.1:n.-8_-7del
NM_001302753.2:c.-8_-7del	NP_001289682.1:n.-8_-7del
NM_001322421.2:c.-8_-7del	NP_001309350.1:n.-8_-7del
NM_001322422.2:c.-8_-7del	NP_001309351.1:n.-8_-7del
NM_001362758.2:c.-8_-7del	NP_001349687.1:n.-8_-7del
NM_152854.4:c.-8_-7del	NP_690593.1:n.-8_-7del
NR_126502.2:n.23_24del
NR_136327.2:n.23_24del