Canonical Allele Identifier: CA860742123

Gene: ADAMTS13

Linked Data

• dbSNP Id: rs1338550562
• gnomAD v3: 9-133454481-G-A
• gnomAD v4: 9-133454481-G-A
• MyVariant Identifiers: chr9:g.133454481G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454481G>A , CM000671.2:g.133454481G>A	GRCh38
NC_000009.10:g.135309424G>A	NCBI36
NG_011934.2:g.45143G>A , LRG_544:g.45143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3111G>A MANE Select	ENSP00000347927.2:p.Val1037=
ENST00000355699.6:c.3111G>A	ENSP00000347927.2:p.Val1037=
ENST00000356589.6:c.3018G>A	ENSP00000348997.2:p.Val1006=
ENST00000371916.5:c.*580G>A	ENSP00000360984.2:n.*580G>A
ENST00000371929.7:c.3111G>A	ENSP00000360997.3:p.Val1037=
ENST00000485925.5:n.1927G>A
NM_139025.4:c.3111G>A , LRG_544t1:c.3111G>A	NP_620594.1:p.Val1037=
NM_139026.4:c.3018G>A	NP_620595.1:p.Val1006=
NM_139027.4:c.3111G>A	NP_620596.2:p.Val1037=
NR_024514.2:n.1946G>A
XM_011518174.1:c.2721G>A	XP_011516476.1:p.Val907=
XM_011518175.1:c.3111G>A	XP_011516477.1:p.Val1037=
XM_011518176.1:c.2127G>A	XP_011516478.1:p.Val709=
XM_011518177.1:c.2121G>A	XP_011516479.1:p.Val707=
XM_011518178.1:c.1776G>A	XP_011516480.1:p.Val592=
XM_011518179.1:c.1776G>A	XP_011516481.1:p.Val592=
XM_011518180.1:c.1377G>A	XP_011516482.1:p.Val459=
XM_011518176.3:c.2127G>A	XP_011516478.1:p.Val709=
XM_011518178.2:c.1776G>A	XP_011516480.1:p.Val592=
XM_017014232.1:c.3099G>A	XP_016869721.1:p.Val1033=
XM_017014233.1:c.2721G>A	XP_016869722.1:p.Val907=
XM_017014234.2:c.2121G>A	XP_016869723.1:p.Val707=
NM_139026.5:c.3018G>A	NP_620595.1:p.Val1006=
NM_139027.5:c.3111G>A	NP_620596.2:p.Val1037=
NM_139025.5:c.3111G>A	NP_620594.1:p.Val1037=
NM_139026.6:c.3018G>A	NP_620595.1:p.Val1006=
NM_139027.6:c.3111G>A MANE Select	NP_620596.2:p.Val1037=
NR_024514.3:n.1948G>A