Canonical Allele Identifier: CA2366533118

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128249_46128250delinsTG , CM000682.2:g.46128249_46128250delinsTG	GRCh38
NC_000020.10:g.44756888_44756889delinsTG , CM000682.1:g.44756888_44756889delinsTG	GRCh37
NC_000020.9:g.44190295_44190296delinsTG	NCBI36
NG_007279.1:g.14983_14984delinsTG , LRG_40:g.14983_14984delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.648+25_648+26delinsTG	ENSP00000512095.1:n.648+25_648+26delinsTG
ENST00000489304.6:c.729+25_729+26delinsTG	ENSP00000512096.1:n.729+25_729+26delinsTG
ENST00000695670.1:n.627+13_627+14delinsTG
ENST00000695671.1:c.686+25_686+26delinsTG	ENSP00000512093.1:n.686+25_686+26delinsTG
ENST00000695674.1:n.1125+25_1125+26delinsTG
ENST00000695675.1:n.2522+25_2522+26delinsTG
ENST00000372285.8:c.646+25_646+26delinsTG MANE Select	ENSP00000361359.3:n.646+25_646+26delinsTG
ENST00000372276.7:c.584+25_584+26delinsTG	ENSP00000361350.3:n.584+25_584+26delinsTG
ENST00000372285.7:c.646+25_646+26delinsTG	ENSP00000361359.3:n.646+25_646+26delinsTG
ENST00000466205.5:c.548+25_548+26delinsTG
ENST00000477696.5:n.619+25_619+26delinsTG
ENST00000489304.5:n.722+25_722+26delinsTG
ENST00000620709.4:c.*193+25_*193+26delinsTG	ENSP00000484074.1:n.*193+25_*193+26delinsTG
NM_001250.5:c.646+25_646+26delinsTG	NP_001241.1:n.646+25_646+26delinsTG
NM_001302753.1:c.686+25_686+26delinsTG	NP_001289682.1:n.686+25_686+26delinsTG
NM_152854.3:c.584+25_584+26delinsTG	NP_690593.1:n.584+25_584+26delinsTG
NR_126502.1:n.739+25_739+26delinsTG
XM_005260617.2:c.658+13_658+14delinsTG	XP_005260674.1:n.658+13_658+14delinsTG
XM_005260619.2:c.502+13_502+14delinsTG	XP_005260676.1:n.502+13_502+14delinsTG
XR_936660.1:n.646+25_646+26delinsTG
NM_001322421.1:c.658+13_658+14delinsTG	NP_001309350.1:n.658+13_658+14delinsTG
NM_001322422.1:c.490+25_490+26delinsTG	NP_001309351.1:n.490+25_490+26delinsTG
NM_001362758.1:c.646+25_646+26delinsTG	NP_001349687.1:n.646+25_646+26delinsTG
NR_136327.1:n.642+25_642+26delinsTG
XM_005260619.3:c.502+13_502+14delinsTG	XP_005260676.1:n.502+13_502+14delinsTG
XM_017028135.1:c.686+25_686+26delinsTG	XP_016883624.1:n.686+25_686+26delinsTG
XM_017028136.1:c.584+25_584+26delinsTG	XP_016883625.1:n.584+25_584+26delinsTG
NM_001250.6:c.646+25_646+26delinsTG MANE Select	NP_001241.1:n.646+25_646+26delinsTG
NM_001302753.2:c.686+25_686+26delinsTG	NP_001289682.1:n.686+25_686+26delinsTG
NM_001322421.2:c.658+13_658+14delinsTG	NP_001309350.1:n.658+13_658+14delinsTG
NM_001322422.2:c.490+25_490+26delinsTG	NP_001309351.1:n.490+25_490+26delinsTG
NM_001362758.2:c.646+25_646+26delinsTG	NP_001349687.1:n.646+25_646+26delinsTG
NM_152854.4:c.584+25_584+26delinsTG	NP_690593.1:n.584+25_584+26delinsTG
NR_126502.2:n.679+25_679+26delinsTG
NR_136327.2:n.582+25_582+26delinsTG