Canonical Allele Identifier: CA1882681576

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454389_133454401delinsCTCTCTGGGGTCT , CM000671.2:g.133454389_133454401delinsCTCTCTGGGGTCT	GRCh38
NC_000009.10:g.135309332_135309344delinsCTCTCTGGGGTCT	NCBI36
NG_011934.2:g.45051_45063delinsCTCTCTGGGGTCT , LRG_544:g.45051_45063delinsCTCTCTGGGGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3045-26_3045-14delinsCTCTCTGGGGTCT MANE Select	ENSP00000347927.2:n.3045-26_3045-14delinsCTCTCTGGGGTCT
ENST00000355699.6:c.3045-26_3045-14delinsCTCTCTGGGGTCT	ENSP00000347927.2:n.3045-26_3045-14delinsCTCTCTGGGGTCT
ENST00000356589.6:c.2952-26_2952-14delinsCTCTCTGGGGTCT	ENSP00000348997.2:n.2952-26_2952-14delinsCTCTCTGGGGTCT
ENST00000371916.5:c.*514-26_*514-14delinsCTCTCTGGGGTCT	ENSP00000360984.2:n.*514-26_*514-14delinsCTCTCTGGGGTCT
ENST00000371929.7:c.3045-26_3045-14delinsCTCTCTGGGGTCT	ENSP00000360997.3:n.3045-26_3045-14delinsCTCTCTGGGGTCT
ENST00000485925.5:n.1861-26_1861-14delinsCTCTCTGGGGTCT
NM_139025.4:c.3045-26_3045-14delinsCTCTCTGGGGTCT , LRG_544t1:c.3045-26_3045-14delinsCTCTCTGGGGTCT	NP_620594.1:n.3045-26_3045-14delinsCTCTCTGGGGTCT
NM_139026.4:c.2952-26_2952-14delinsCTCTCTGGGGTCT	NP_620595.1:n.2952-26_2952-14delinsCTCTCTGGGGTCT
NM_139027.4:c.3045-26_3045-14delinsCTCTCTGGGGTCT	NP_620596.2:n.3045-26_3045-14delinsCTCTCTGGGGTCT
NR_024514.2:n.1880-26_1880-14delinsCTCTCTGGGGTCT
XM_011518174.1:c.2655-26_2655-14delinsCTCTCTGGGGTCT	XP_011516476.1:n.2655-26_2655-14delinsCTCTCTGGGGTCT
XM_011518175.1:c.3045-26_3045-14delinsCTCTCTGGGGTCT	XP_011516477.1:n.3045-26_3045-14delinsCTCTCTGGGGTCT
XM_011518176.1:c.2061-26_2061-14delinsCTCTCTGGGGTCT	XP_011516478.1:n.2061-26_2061-14delinsCTCTCTGGGGTCT
XM_011518177.1:c.2055-26_2055-14delinsCTCTCTGGGGTCT	XP_011516479.1:n.2055-26_2055-14delinsCTCTCTGGGGTCT
XM_011518178.1:c.1710-26_1710-14delinsCTCTCTGGGGTCT	XP_011516480.1:n.1710-26_1710-14delinsCTCTCTGGGGTCT
XM_011518179.1:c.1710-26_1710-14delinsCTCTCTGGGGTCT	XP_011516481.1:n.1710-26_1710-14delinsCTCTCTGGGGTCT
XM_011518180.1:c.1311-26_1311-14delinsCTCTCTGGGGTCT	XP_011516482.1:n.1311-26_1311-14delinsCTCTCTGGGGTCT
XM_011518176.3:c.2061-26_2061-14delinsCTCTCTGGGGTCT	XP_011516478.1:n.2061-26_2061-14delinsCTCTCTGGGGTCT
XM_011518178.2:c.1710-26_1710-14delinsCTCTCTGGGGTCT	XP_011516480.1:n.1710-26_1710-14delinsCTCTCTGGGGTCT
XM_017014232.1:c.3033-26_3033-14delinsCTCTCTGGGGTCT	XP_016869721.1:n.3033-26_3033-14delinsCTCTCTGGGGTCT
XM_017014233.1:c.2655-26_2655-14delinsCTCTCTGGGGTCT	XP_016869722.1:n.2655-26_2655-14delinsCTCTCTGGGGTCT
XM_017014234.2:c.2055-26_2055-14delinsCTCTCTGGGGTCT	XP_016869723.1:n.2055-26_2055-14delinsCTCTCTGGGGTCT
XR_001746171.1:n.3818-26_3818-14delinsCTCTCTGGGGTCT
NM_139026.5:c.2952-26_2952-14delinsCTCTCTGGGGTCT	NP_620595.1:n.2952-26_2952-14delinsCTCTCTGGGGTCT
NM_139027.5:c.3045-26_3045-14delinsCTCTCTGGGGTCT	NP_620596.2:n.3045-26_3045-14delinsCTCTCTGGGGTCT
NM_139025.5:c.3045-26_3045-14delinsCTCTCTGGGGTCT	NP_620594.1:n.3045-26_3045-14delinsCTCTCTGGGGTCT
NM_139026.6:c.2952-26_2952-14delinsCTCTCTGGGGTCT	NP_620595.1:n.2952-26_2952-14delinsCTCTCTGGGGTCT
NM_139027.6:c.3045-26_3045-14delinsCTCTCTGGGGTCT MANE Select	NP_620596.2:n.3045-26_3045-14delinsCTCTCTGGGGTCT
NR_024514.3:n.1882-26_1882-14delinsCTCTCTGGGGTCT