Canonical Allele Identifier: CA2554746124

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129201_46129202insCA , CM000682.2:g.46129201_46129202insCA	GRCh38
NC_000020.10:g.44757840_44757841insCA , CM000682.1:g.44757840_44757841insCA	GRCh37
NC_000020.9:g.44191247_44191248insCA	NCBI36
NG_007279.1:g.15935_15936insCA , LRG_40:g.15935_15936insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1078_1079insCA	ENSP00000512096.1:n.1078_1079insCA
ENST00000695675.1:n.2871_2872insCA
ENST00000372285.8:c.*161_*162insCA MANE Select	ENSP00000361359.3:n.*161_*162insCA
ENST00000372276.7:c.*321_*322insCA	ENSP00000361350.3:n.*321_*322insCA
ENST00000372285.7:c.*161_*162insCA	ENSP00000361359.3:n.*161_*162insCA
ENST00000489304.5:n.1071_1072insCA
ENST00000620709.4:c.*542_*543insCA	ENSP00000484074.1:n.*542_*543insCA
NM_001250.5:c.*161_*162insCA	NP_001241.1:n.*161_*162insCA
NM_001302753.1:c.*321_*322insCA	NP_001289682.1:n.*321_*322insCA
NM_152854.3:c.*321_*322insCA	NP_690593.1:n.*321_*322insCA
NR_126502.1:n.1088_1089insCA
XM_005260617.2:c.*161_*162insCA	XP_005260674.1:n.*161_*162insCA
XM_005260619.2:c.*161_*162insCA	XP_005260676.1:n.*161_*162insCA
NM_001322421.1:c.*161_*162insCA	NP_001309350.1:n.*161_*162insCA
NM_001322422.1:c.*161_*162insCA	NP_001309351.1:n.*161_*162insCA
NM_001362758.1:c.*321_*322insCA	NP_001349687.1:n.*321_*322insCA
NR_136327.1:n.991_992insCA
XM_005260619.3:c.*161_*162insCA	XP_005260676.1:n.*161_*162insCA
XM_017028135.1:c.*58_*59insCA	XP_016883624.1:n.*58_*59insCA
XM_017028136.1:c.*58_*59insCA	XP_016883625.1:n.*58_*59insCA
NM_001250.6:c.*161_*162insCA MANE Select	NP_001241.1:n.*161_*162insCA
NM_001302753.2:c.*321_*322insCA	NP_001289682.1:n.*321_*322insCA
NM_001322421.2:c.*161_*162insCA	NP_001309350.1:n.*161_*162insCA
NM_001322422.2:c.*161_*162insCA	NP_001309351.1:n.*161_*162insCA
NM_001362758.2:c.*321_*322insCA	NP_001349687.1:n.*321_*322insCA
NM_152854.4:c.*321_*322insCA	NP_690593.1:n.*321_*322insCA
NR_126502.2:n.1028_1029insCA
NR_136327.2:n.931_932insCA