Canonical Allele Identifier: CA2692373003

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133448705-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133448705C>T , CM000671.2:g.133448705C>T	GRCh38
NC_000009.10:g.135303647C>T	NCBI36
NG_011934.2:g.39367C>T , LRG_544:g.39367C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2838C>T MANE Select	ENSP00000347927.2:p.Cys946=
ENST00000355699.6:c.2838C>T	ENSP00000347927.2:p.Cys946=
ENST00000356589.6:c.2745C>T	ENSP00000348997.2:p.Cys915=
ENST00000371916.5:c.*307C>T	ENSP00000360984.2:n.*307C>T
ENST00000371929.7:c.2838C>T	ENSP00000360997.3:p.Cys946=
ENST00000485925.5:n.1654C>T
ENST00000495234.5:c.*1670C>T	ENSP00000435274.1:n.*1670C>T
NM_139025.4:c.2838C>T , LRG_544t1:c.2838C>T	NP_620594.1:p.Cys946=
NM_139026.4:c.2745C>T	NP_620595.1:p.Cys915=
NM_139027.4:c.2838C>T	NP_620596.2:p.Cys946=
NR_024514.2:n.1673C>T
XM_011518174.1:c.2448C>T	XP_011516476.1:p.Cys816=
XM_011518175.1:c.2838C>T	XP_011516477.1:p.Cys946=
XM_011518176.1:c.1854C>T	XP_011516478.1:p.Cys618=
XM_011518177.1:c.1848C>T	XP_011516479.1:p.Cys616=
XM_011518178.1:c.1503C>T	XP_011516480.1:p.Cys501=
XM_011518179.1:c.1503C>T	XP_011516481.1:p.Cys501=
XM_011518180.1:c.1104C>T	XP_011516482.1:p.Cys368=
XM_011518176.3:c.1854C>T	XP_011516478.1:p.Cys618=
XM_011518178.2:c.1503C>T	XP_011516480.1:p.Cys501=
XM_017014232.1:c.2826C>T	XP_016869721.1:p.Cys942=
XM_017014233.1:c.2448C>T	XP_016869722.1:p.Cys816=
XM_017014234.2:c.1848C>T	XP_016869723.1:p.Cys616=
XR_001746171.1:n.3611C>T
NM_139026.5:c.2745C>T	NP_620595.1:p.Cys915=
NM_139027.5:c.2838C>T	NP_620596.2:p.Cys946=
NM_139025.5:c.2838C>T	NP_620594.1:p.Cys946=
NM_139026.6:c.2745C>T	NP_620595.1:p.Cys915=
NM_139027.6:c.2838C>T MANE Select	NP_620596.2:p.Cys946=
NR_024514.3:n.1675C>T