Canonical Allele Identifier: CA2838152193

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454520G>C , CM000671.2:g.133454520G>C	GRCh38
NC_000009.10:g.135309463G>C	NCBI36
NG_011934.2:g.45182G>C , LRG_544:g.45182G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3150G>C MANE Select	ENSP00000347927.2:p.Val1050=
ENST00000355699.6:c.3150G>C	ENSP00000347927.2:p.Val1050=
ENST00000356589.6:c.3057G>C	ENSP00000348997.2:p.Val1019=
ENST00000371916.5:c.*619G>C	ENSP00000360984.2:n.*619G>C
ENST00000371929.7:c.3150G>C	ENSP00000360997.3:p.Val1050=
ENST00000485925.5:n.1966G>C
NM_139025.4:c.3150G>C , LRG_544t1:c.3150G>C	NP_620594.1:p.Val1050=
NM_139026.4:c.3057G>C	NP_620595.1:p.Val1019=
NM_139027.4:c.3150G>C	NP_620596.2:p.Val1050=
NR_024514.2:n.1985G>C
XM_011518174.1:c.2760G>C	XP_011516476.1:p.Val920=
XM_011518175.1:c.3150G>C	XP_011516477.1:p.Val1050=
XM_011518176.1:c.2166G>C	XP_011516478.1:p.Val722=
XM_011518177.1:c.2160G>C	XP_011516479.1:p.Val720=
XM_011518178.1:c.1815G>C	XP_011516480.1:p.Val605=
XM_011518179.1:c.1815G>C	XP_011516481.1:p.Val605=
XM_011518180.1:c.1416G>C	XP_011516482.1:p.Val472=
XM_011518176.3:c.2166G>C	XP_011516478.1:p.Val722=
XM_011518178.2:c.1815G>C	XP_011516480.1:p.Val605=
XM_017014232.1:c.3138G>C	XP_016869721.1:p.Val1046=
XM_017014233.1:c.2760G>C	XP_016869722.1:p.Val920=
XM_017014234.2:c.2160G>C	XP_016869723.1:p.Val720=
NM_139026.5:c.3057G>C	NP_620595.1:p.Val1019=
NM_139027.5:c.3150G>C	NP_620596.2:p.Val1050=
NM_139025.5:c.3150G>C	NP_620594.1:p.Val1050=
NM_139026.6:c.3057G>C	NP_620595.1:p.Val1019=
NM_139027.6:c.3150G>C MANE Select	NP_620596.2:p.Val1050=
NR_024514.3:n.1987G>C