Canonical Allele Identifier: CA375410069

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454438C>A , CM000671.2:g.133454438C>A	GRCh38
NC_000009.10:g.135309381C>A	NCBI36
NG_011934.2:g.45100C>A , LRG_544:g.45100C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3068C>A MANE Select	ENSP00000347927.2:p.Pro1023Gln
ENST00000355699.6:c.3068C>A	ENSP00000347927.2:p.Pro1023Gln
ENST00000356589.6:c.2975C>A	ENSP00000348997.2:p.Pro992Gln
ENST00000371916.5:c.*537C>A	ENSP00000360984.2:n.*537C>A
ENST00000371929.7:c.3068C>A	ENSP00000360997.3:p.Pro1023Gln
ENST00000485925.5:n.1884C>A
NM_139025.4:c.3068C>A , LRG_544t1:c.3068C>A	NP_620594.1:p.Pro1023Gln
NM_139026.4:c.2975C>A	NP_620595.1:p.Pro992Gln
NM_139027.4:c.3068C>A	NP_620596.2:p.Pro1023Gln
NR_024514.2:n.1903C>A
XM_011518174.1:c.2678C>A	XP_011516476.1:p.Pro893Gln
XM_011518175.1:c.3068C>A	XP_011516477.1:p.Pro1023Gln
XM_011518176.1:c.2084C>A	XP_011516478.1:p.Pro695Gln
XM_011518177.1:c.2078C>A	XP_011516479.1:p.Pro693Gln
XM_011518178.1:c.1733C>A	XP_011516480.1:p.Pro578Gln
XM_011518179.1:c.1733C>A	XP_011516481.1:p.Pro578Gln
XM_011518180.1:c.1334C>A	XP_011516482.1:p.Pro445Gln
XM_011518176.3:c.2084C>A	XP_011516478.1:p.Pro695Gln
XM_011518178.2:c.1733C>A	XP_011516480.1:p.Pro578Gln
XM_017014232.1:c.3056C>A	XP_016869721.1:p.Pro1019Gln
XM_017014233.1:c.2678C>A	XP_016869722.1:p.Pro893Gln
XM_017014234.2:c.2078C>A	XP_016869723.1:p.Pro693Gln
XR_001746171.1:n.3841C>A
NM_139026.5:c.2975C>A	NP_620595.1:p.Pro992Gln
NM_139027.5:c.3068C>A	NP_620596.2:p.Pro1023Gln
NM_139025.5:c.3068C>A	NP_620594.1:p.Pro1023Gln
NM_139026.6:c.2975C>A	NP_620595.1:p.Pro992Gln
NM_139027.6:c.3068C>A MANE Select	NP_620596.2:p.Pro1023Gln
NR_024514.3:n.1905C>A