Canonical Allele Identifier: CA1882673208

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436993_133436994delinsGC , CM000671.2:g.133436993_133436994delinsGC	GRCh38
NC_000009.10:g.135291934_135291935delinsGC	NCBI36
NG_011934.2:g.27655_27656delinsGC , LRG_544:g.27655_27656delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1435+38_1435+39delinsGC MANE Select	ENSP00000347927.2:n.1435+38_1435+39delinsGC
ENST00000355699.6:c.1435+38_1435+39delinsGC	ENSP00000347927.2:n.1435+38_1435+39delinsGC
ENST00000356589.6:c.1342+38_1342+39delinsGC	ENSP00000348997.2:n.1342+38_1342+39delinsGC
ENST00000371916.5:c.691+38_691+39delinsGC	ENSP00000360984.2:n.691+38_691+39delinsGC
ENST00000371929.7:c.1435+38_1435+39delinsGC	ENSP00000360997.3:n.1435+38_1435+39delinsGC
ENST00000474918.1:c.*239+38_*239+39delinsGC	ENSP00000435305.1:n.*239+38_*239+39delinsGC
ENST00000485925.5:n.974-2373_974-2372delinsGC
ENST00000495234.5:c.*719+38_*719+39delinsGC	ENSP00000435274.1:n.*719+38_*719+39delinsGC
NM_139025.4:c.1435+38_1435+39delinsGC , LRG_544t1:c.1435+38_1435+39delinsGC	NP_620594.1:n.1435+38_1435+39delinsGC
NM_139026.4:c.1342+38_1342+39delinsGC	NP_620595.1:n.1342+38_1342+39delinsGC
NM_139027.4:c.1435+38_1435+39delinsGC	NP_620596.2:n.1435+38_1435+39delinsGC
NR_024514.2:n.993-2373_993-2372delinsGC
XM_011518174.1:c.1045+38_1045+39delinsGC	XP_011516476.1:n.1045+38_1045+39delinsGC
XM_011518175.1:c.1435+38_1435+39delinsGC	XP_011516477.1:n.1435+38_1435+39delinsGC
XM_011518176.1:c.451+38_451+39delinsGC	XP_011516478.1:n.451+38_451+39delinsGC
XM_011518177.1:c.445+38_445+39delinsGC	XP_011516479.1:n.445+38_445+39delinsGC
XM_011518178.1:c.100+38_100+39delinsGC	XP_011516480.1:n.100+38_100+39delinsGC
XM_011518179.1:c.221+38_221+39delinsGC	XP_011516481.1:n.221+38_221+39delinsGC
XM_011518180.1:c.687-7870_687-7869delinsGC	XP_011516482.1:n.687-7870_687-7869delinsGC
XM_011518176.3:c.451+38_451+39delinsGC	XP_011516478.1:n.451+38_451+39delinsGC
XM_011518178.2:c.100+38_100+39delinsGC	XP_011516480.1:n.100+38_100+39delinsGC
XM_017014232.1:c.1423+38_1423+39delinsGC	XP_016869721.1:n.1423+38_1423+39delinsGC
XM_017014233.1:c.1045+38_1045+39delinsGC	XP_016869722.1:n.1045+38_1045+39delinsGC
XM_017014234.2:c.445+38_445+39delinsGC	XP_016869723.1:n.445+38_445+39delinsGC
XM_017014235.1:c.1435+38_1435+39delinsGC	XP_016869724.1:n.1435+38_1435+39delinsGC
XR_001746171.1:n.2660+38_2660+39delinsGC
NM_139026.5:c.1342+38_1342+39delinsGC	NP_620595.1:n.1342+38_1342+39delinsGC
NM_139027.5:c.1435+38_1435+39delinsGC	NP_620596.2:n.1435+38_1435+39delinsGC
NM_139025.5:c.1435+38_1435+39delinsGC	NP_620594.1:n.1435+38_1435+39delinsGC
NM_139026.6:c.1342+38_1342+39delinsGC	NP_620595.1:n.1342+38_1342+39delinsGC
NM_139027.6:c.1435+38_1435+39delinsGC MANE Select	NP_620596.2:n.1435+38_1435+39delinsGC
NR_024514.3:n.995-2373_995-2372delinsGC