Canonical Allele Identifier: CA375410130

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454451C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454451C>A , CM000671.2:g.133454451C>A	GRCh38
NC_000009.10:g.135309394C>A	NCBI36
NG_011934.2:g.45113C>A , LRG_544:g.45113C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.3081C>A MANE Select	ENSP00000347927.2:p.Ser1027Arg
ENST00000355699.6:c.3081C>A	ENSP00000347927.2:p.Ser1027Arg
ENST00000356589.6:c.2988C>A	ENSP00000348997.2:p.Ser996Arg
ENST00000371916.5:c.*550C>A	ENSP00000360984.2:n.*550C>A
ENST00000371929.7:c.3081C>A	ENSP00000360997.3:p.Ser1027Arg
ENST00000485925.5:n.1897C>A
NM_139025.4:c.3081C>A , LRG_544t1:c.3081C>A	NP_620594.1:p.Ser1027Arg
NM_139026.4:c.2988C>A	NP_620595.1:p.Ser996Arg
NM_139027.4:c.3081C>A	NP_620596.2:p.Ser1027Arg
NR_024514.2:n.1916C>A
XM_011518174.1:c.2691C>A	XP_011516476.1:p.Ser897Arg
XM_011518175.1:c.3081C>A	XP_011516477.1:p.Ser1027Arg
XM_011518176.1:c.2097C>A	XP_011516478.1:p.Ser699Arg
XM_011518177.1:c.2091C>A	XP_011516479.1:p.Ser697Arg
XM_011518178.1:c.1746C>A	XP_011516480.1:p.Ser582Arg
XM_011518179.1:c.1746C>A	XP_011516481.1:p.Ser582Arg
XM_011518180.1:c.1347C>A	XP_011516482.1:p.Ser449Arg
XM_011518176.3:c.2097C>A	XP_011516478.1:p.Ser699Arg
XM_011518178.2:c.1746C>A	XP_011516480.1:p.Ser582Arg
XM_017014232.1:c.3069C>A	XP_016869721.1:p.Ser1023Arg
XM_017014233.1:c.2691C>A	XP_016869722.1:p.Ser897Arg
XM_017014234.2:c.2091C>A	XP_016869723.1:p.Ser697Arg
XR_001746171.1:n.3854C>A
NM_139026.5:c.2988C>A	NP_620595.1:p.Ser996Arg
NM_139027.5:c.3081C>A	NP_620596.2:p.Ser1027Arg
NM_139025.5:c.3081C>A	NP_620594.1:p.Ser1027Arg
NM_139026.6:c.2988C>A	NP_620595.1:p.Ser996Arg
NM_139027.6:c.3081C>A MANE Select	NP_620596.2:p.Ser1027Arg
NR_024514.3:n.1918C>A