Canonical Allele Identifier: CA860741914
Gene: ADAMTS13 HGNC NCBI

Linked Data

dbSNP Id: rs1428637991
MyVariant Identifiers: chr9:g.133454330T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133454330T>C , CM000671.2:g.133454330T>C GRCh38
NC_000009.10:g.135309273T>C NCBI36
NG_011934.2:g.44992T>C , LRG_544:g.44992T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355699.7:c.3045-85T>C MANE Select ENSP00000347927.2:n.3045-85T>C
ENST00000355699.6:c.3045-85T>C ENSP00000347927.2:n.3045-85T>C
ENST00000356589.6:c.2952-85T>C ENSP00000348997.2:n.2952-85T>C
ENST00000371916.5:c.*514-85T>C ENSP00000360984.2:n.*514-85T>C
ENST00000371929.7:c.3045-85T>C ENSP00000360997.3:n.3045-85T>C
ENST00000485925.5:n.1861-85T>C
NM_139025.4:c.3045-85T>C , LRG_544t1:c.3045-85T>C NP_620594.1:n.3045-85T>C
NM_139026.4:c.2952-85T>C NP_620595.1:n.2952-85T>C
NM_139027.4:c.3045-85T>C NP_620596.2:n.3045-85T>C
NR_024514.2:n.1880-85T>C
XM_011518174.1:c.2655-85T>C XP_011516476.1:n.2655-85T>C
XM_011518175.1:c.3045-85T>C XP_011516477.1:n.3045-85T>C
XM_011518176.1:c.2061-85T>C XP_011516478.1:n.2061-85T>C
XM_011518177.1:c.2055-85T>C XP_011516479.1:n.2055-85T>C
XM_011518178.1:c.1710-85T>C XP_011516480.1:n.1710-85T>C
XM_011518179.1:c.1710-85T>C XP_011516481.1:n.1710-85T>C
XM_011518180.1:c.1311-85T>C XP_011516482.1:n.1311-85T>C
XM_011518176.3:c.2061-85T>C XP_011516478.1:n.2061-85T>C
XM_011518178.2:c.1710-85T>C XP_011516480.1:n.1710-85T>C
XM_017014232.1:c.3033-85T>C XP_016869721.1:n.3033-85T>C
XM_017014233.1:c.2655-85T>C XP_016869722.1:n.2655-85T>C
XM_017014234.2:c.2055-85T>C XP_016869723.1:n.2055-85T>C
XR_001746171.1:n.3818-85T>C
NM_139026.5:c.2952-85T>C NP_620595.1:n.2952-85T>C
NM_139027.5:c.3045-85T>C NP_620596.2:n.3045-85T>C
NM_139025.5:c.3045-85T>C NP_620594.1:n.3045-85T>C
NM_139026.6:c.2952-85T>C NP_620595.1:n.2952-85T>C
NM_139027.6:c.3045-85T>C MANE Select NP_620596.2:n.3045-85T>C
NR_024514.3:n.1882-85T>C