Canonical Allele Identifier: CA375410933

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133454611-T-C
• MyVariant Identifiers: chr9:g.133454611T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454611T>C , CM000671.2:g.133454611T>C	GRCh38
NC_000009.10:g.135309554T>C	NCBI36
NG_011934.2:g.45273T>C , LRG_544:g.45273T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3241T>C MANE Select	ENSP00000347927.2:p.Trp1081Arg
ENST00000355699.6:c.3241T>C	ENSP00000347927.2:p.Trp1081Arg
ENST00000356589.6:c.3148T>C	ENSP00000348997.2:p.Trp1050Arg
ENST00000371916.5:c.*710T>C	ENSP00000360984.2:n.*710T>C
ENST00000371929.7:c.3241T>C	ENSP00000360997.3:p.Trp1081Arg
ENST00000485925.5:n.2057T>C
NM_139025.4:c.3241T>C , LRG_544t1:c.3241T>C	NP_620594.1:p.Trp1081Arg
NM_139026.4:c.3148T>C	NP_620595.1:p.Trp1050Arg
NM_139027.4:c.3241T>C	NP_620596.2:p.Trp1081Arg
NR_024514.2:n.2076T>C
XM_011518174.1:c.2851T>C	XP_011516476.1:p.Trp951Arg
XM_011518175.1:c.3241T>C	XP_011516477.1:p.Trp1081Arg
XM_011518176.1:c.2257T>C	XP_011516478.1:p.Trp753Arg
XM_011518177.1:c.2251T>C	XP_011516479.1:p.Trp751Arg
XM_011518178.1:c.1906T>C	XP_011516480.1:p.Trp636Arg
XM_011518179.1:c.1906T>C	XP_011516481.1:p.Trp636Arg
XM_011518180.1:c.1507T>C	XP_011516482.1:p.Trp503Arg
XM_011518176.3:c.2257T>C	XP_011516478.1:p.Trp753Arg
XM_011518178.2:c.1906T>C	XP_011516480.1:p.Trp636Arg
XM_017014232.1:c.3229T>C	XP_016869721.1:p.Trp1077Arg
XM_017014233.1:c.2851T>C	XP_016869722.1:p.Trp951Arg
XM_017014234.2:c.2251T>C	XP_016869723.1:p.Trp751Arg
NM_139026.5:c.3148T>C	NP_620595.1:p.Trp1050Arg
NM_139027.5:c.3241T>C	NP_620596.2:p.Trp1081Arg
NM_139025.5:c.3241T>C	NP_620594.1:p.Trp1081Arg
NM_139026.6:c.3148T>C	NP_620595.1:p.Trp1050Arg
NM_139027.6:c.3241T>C MANE Select	NP_620596.2:p.Trp1081Arg
NR_024514.3:n.2078T>C