Canonical Allele Identifier: CA1882673224

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133437025_133437026delinsAG , CM000671.2:g.133437025_133437026delinsAG	GRCh38
NC_000009.10:g.135291966_135291967delinsAG	NCBI36
NG_011934.2:g.27687_27688delinsAG , LRG_544:g.27687_27688delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1435+70_1435+71delinsAG MANE Select	ENSP00000347927.2:n.1435+70_1435+71delinsAG
ENST00000355699.6:c.1435+70_1435+71delinsAG	ENSP00000347927.2:n.1435+70_1435+71delinsAG
ENST00000356589.6:c.1342+70_1342+71delinsAG	ENSP00000348997.2:n.1342+70_1342+71delinsAG
ENST00000371916.5:c.691+70_691+71delinsAG	ENSP00000360984.2:n.691+70_691+71delinsAG
ENST00000371929.7:c.1435+70_1435+71delinsAG	ENSP00000360997.3:n.1435+70_1435+71delinsAG
ENST00000474918.1:c.*239+70_*239+71delinsAG	ENSP00000435305.1:n.*239+70_*239+71delinsAG
ENST00000485925.5:n.974-2341_974-2340delinsAG
ENST00000495234.5:c.*719+70_*719+71delinsAG	ENSP00000435274.1:n.*719+70_*719+71delinsAG
NM_139025.4:c.1435+70_1435+71delinsAG , LRG_544t1:c.1435+70_1435+71delinsAG	NP_620594.1:n.1435+70_1435+71delinsAG
NM_139026.4:c.1342+70_1342+71delinsAG	NP_620595.1:n.1342+70_1342+71delinsAG
NM_139027.4:c.1435+70_1435+71delinsAG	NP_620596.2:n.1435+70_1435+71delinsAG
NR_024514.2:n.993-2341_993-2340delinsAG
XM_011518174.1:c.1045+70_1045+71delinsAG	XP_011516476.1:n.1045+70_1045+71delinsAG
XM_011518175.1:c.1435+70_1435+71delinsAG	XP_011516477.1:n.1435+70_1435+71delinsAG
XM_011518176.1:c.451+70_451+71delinsAG	XP_011516478.1:n.451+70_451+71delinsAG
XM_011518177.1:c.445+70_445+71delinsAG	XP_011516479.1:n.445+70_445+71delinsAG
XM_011518178.1:c.100+70_100+71delinsAG	XP_011516480.1:n.100+70_100+71delinsAG
XM_011518179.1:c.221+70_221+71delinsAG	XP_011516481.1:n.221+70_221+71delinsAG
XM_011518180.1:c.687-7838_687-7837delinsAG	XP_011516482.1:n.687-7838_687-7837delinsAG
XM_011518176.3:c.451+70_451+71delinsAG	XP_011516478.1:n.451+70_451+71delinsAG
XM_011518178.2:c.100+70_100+71delinsAG	XP_011516480.1:n.100+70_100+71delinsAG
XM_017014232.1:c.1423+70_1423+71delinsAG	XP_016869721.1:n.1423+70_1423+71delinsAG
XM_017014233.1:c.1045+70_1045+71delinsAG	XP_016869722.1:n.1045+70_1045+71delinsAG
XM_017014234.2:c.445+70_445+71delinsAG	XP_016869723.1:n.445+70_445+71delinsAG
XM_017014235.1:c.1435+70_1435+71delinsAG	XP_016869724.1:n.1435+70_1435+71delinsAG
XR_001746171.1:n.2660+70_2660+71delinsAG
NM_139026.5:c.1342+70_1342+71delinsAG	NP_620595.1:n.1342+70_1342+71delinsAG
NM_139027.5:c.1435+70_1435+71delinsAG	NP_620596.2:n.1435+70_1435+71delinsAG
NM_139025.5:c.1435+70_1435+71delinsAG	NP_620594.1:n.1435+70_1435+71delinsAG
NM_139026.6:c.1342+70_1342+71delinsAG	NP_620595.1:n.1342+70_1342+71delinsAG
NM_139027.6:c.1435+70_1435+71delinsAG MANE Select	NP_620596.2:n.1435+70_1435+71delinsAG
NR_024514.3:n.995-2341_995-2340delinsAG