Canonical Allele Identifier: CA375391453

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133436841-A-T
• MyVariant Identifiers: chr9:g.133436841A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436841A>T , CM000671.2:g.133436841A>T	GRCh38
NC_000009.10:g.135291782A>T	NCBI36
NG_011934.2:g.27503A>T , LRG_544:g.27503A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1321A>T MANE Select	ENSP00000347927.2:p.Thr441Ser
ENST00000355699.6:c.1321A>T	ENSP00000347927.2:p.Thr441Ser
ENST00000356589.6:c.1228A>T	ENSP00000348997.2:p.Thr410Ser
ENST00000371916.5:c.577A>T	ENSP00000360984.2:p.Thr193Ser
ENST00000371929.7:c.1321A>T	ENSP00000360997.3:p.Thr441Ser
ENST00000474918.1:c.*125A>T	ENSP00000435305.1:n.*125A>T
ENST00000485925.5:n.974-2525A>T
ENST00000495234.5:c.*605A>T	ENSP00000435274.1:n.*605A>T
NM_139025.4:c.1321A>T , LRG_544t1:c.1321A>T	NP_620594.1:p.Thr441Ser
NM_139026.4:c.1228A>T	NP_620595.1:p.Thr410Ser
NM_139027.4:c.1321A>T	NP_620596.2:p.Thr441Ser
NR_024514.2:n.993-2525A>T
XM_011518174.1:c.931A>T	XP_011516476.1:p.Thr311Ser
XM_011518175.1:c.1321A>T	XP_011516477.1:p.Thr441Ser
XM_011518176.1:c.337A>T	XP_011516478.1:p.Thr113Ser
XM_011518177.1:c.331A>T	XP_011516479.1:p.Thr111Ser
XM_011518178.1:c.-15A>T	XP_011516480.1:n.-15A>T
XM_011518179.1:c.107A>T	XP_011516481.1:p.Asp36Val
XM_011518180.1:c.687-8022A>T	XP_011516482.1:n.687-8022A>T
XM_011518176.3:c.337A>T	XP_011516478.1:p.Thr113Ser
XM_011518178.2:c.-15A>T	XP_011516480.1:n.-15A>T
XM_017014232.1:c.1309A>T	XP_016869721.1:p.Thr437Ser
XM_017014233.1:c.931A>T	XP_016869722.1:p.Thr311Ser
XM_017014234.2:c.331A>T	XP_016869723.1:p.Thr111Ser
XM_017014235.1:c.1321A>T	XP_016869724.1:p.Thr441Ser
XR_001746171.1:n.2546A>T
NM_139026.5:c.1228A>T	NP_620595.1:p.Thr410Ser
NM_139027.5:c.1321A>T	NP_620596.2:p.Thr441Ser
NM_139025.5:c.1321A>T	NP_620594.1:p.Thr441Ser
NM_139026.6:c.1228A>T	NP_620595.1:p.Thr410Ser
NM_139027.6:c.1321A>T MANE Select	NP_620596.2:p.Thr441Ser
NR_024514.3:n.995-2525A>T