Canonical Allele Identifier: CA1882681551

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454345_133454346delinsAG , CM000671.2:g.133454345_133454346delinsAG	GRCh38
NC_000009.10:g.135309288_135309289delinsAG	NCBI36
NG_011934.2:g.45007_45008delinsAG , LRG_544:g.45007_45008delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3045-70_3045-69delinsAG MANE Select	ENSP00000347927.2:n.3045-70_3045-69delinsAG
ENST00000355699.6:c.3045-70_3045-69delinsAG	ENSP00000347927.2:n.3045-70_3045-69delinsAG
ENST00000356589.6:c.2952-70_2952-69delinsAG	ENSP00000348997.2:n.2952-70_2952-69delinsAG
ENST00000371916.5:c.*514-70_*514-69delinsAG	ENSP00000360984.2:n.*514-70_*514-69delinsAG
ENST00000371929.7:c.3045-70_3045-69delinsAG	ENSP00000360997.3:n.3045-70_3045-69delinsAG
ENST00000485925.5:n.1861-70_1861-69delinsAG
NM_139025.4:c.3045-70_3045-69delinsAG , LRG_544t1:c.3045-70_3045-69delinsAG	NP_620594.1:n.3045-70_3045-69delinsAG
NM_139026.4:c.2952-70_2952-69delinsAG	NP_620595.1:n.2952-70_2952-69delinsAG
NM_139027.4:c.3045-70_3045-69delinsAG	NP_620596.2:n.3045-70_3045-69delinsAG
NR_024514.2:n.1880-70_1880-69delinsAG
XM_011518174.1:c.2655-70_2655-69delinsAG	XP_011516476.1:n.2655-70_2655-69delinsAG
XM_011518175.1:c.3045-70_3045-69delinsAG	XP_011516477.1:n.3045-70_3045-69delinsAG
XM_011518176.1:c.2061-70_2061-69delinsAG	XP_011516478.1:n.2061-70_2061-69delinsAG
XM_011518177.1:c.2055-70_2055-69delinsAG	XP_011516479.1:n.2055-70_2055-69delinsAG
XM_011518178.1:c.1710-70_1710-69delinsAG	XP_011516480.1:n.1710-70_1710-69delinsAG
XM_011518179.1:c.1710-70_1710-69delinsAG	XP_011516481.1:n.1710-70_1710-69delinsAG
XM_011518180.1:c.1311-70_1311-69delinsAG	XP_011516482.1:n.1311-70_1311-69delinsAG
XM_011518176.3:c.2061-70_2061-69delinsAG	XP_011516478.1:n.2061-70_2061-69delinsAG
XM_011518178.2:c.1710-70_1710-69delinsAG	XP_011516480.1:n.1710-70_1710-69delinsAG
XM_017014232.1:c.3033-70_3033-69delinsAG	XP_016869721.1:n.3033-70_3033-69delinsAG
XM_017014233.1:c.2655-70_2655-69delinsAG	XP_016869722.1:n.2655-70_2655-69delinsAG
XM_017014234.2:c.2055-70_2055-69delinsAG	XP_016869723.1:n.2055-70_2055-69delinsAG
XR_001746171.1:n.3818-70_3818-69delinsAG
NM_139026.5:c.2952-70_2952-69delinsAG	NP_620595.1:n.2952-70_2952-69delinsAG
NM_139027.5:c.3045-70_3045-69delinsAG	NP_620596.2:n.3045-70_3045-69delinsAG
NM_139025.5:c.3045-70_3045-69delinsAG	NP_620594.1:n.3045-70_3045-69delinsAG
NM_139026.6:c.2952-70_2952-69delinsAG	NP_620595.1:n.2952-70_2952-69delinsAG
NM_139027.6:c.3045-70_3045-69delinsAG MANE Select	NP_620596.2:n.3045-70_3045-69delinsAG
NR_024514.3:n.1882-70_1882-69delinsAG