Canonical Allele Identifier: CA1882677297

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133448642G= , CM000671.2:g.133448642G=	GRCh38
NC_000009.10:g.135303584G=	NCBI36
NG_011934.2:g.39304G= , LRG_544:g.39304G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2775G= MANE Select	ENSP00000347927.2:p.Arg925=
ENST00000355699.6:c.2775G=	ENSP00000347927.2:p.Arg925=
ENST00000356589.6:c.2682G=	ENSP00000348997.2:p.Arg894=
ENST00000371916.5:c.*244G=	ENSP00000360984.2:n.*244G=
ENST00000371929.7:c.2775G=	ENSP00000360997.3:p.Arg925=
ENST00000485925.5:n.1591G=
ENST00000495234.5:c.*1607G=	ENSP00000435274.1:n.*1607G=
NM_139025.4:c.2775G= , LRG_544t1:c.2775G=	NP_620594.1:p.Arg925=
NM_139026.4:c.2682G=	NP_620595.1:p.Arg894=
NM_139027.4:c.2775G=	NP_620596.2:p.Arg925=
NR_024514.2:n.1610G=
XM_011518174.1:c.2385G=	XP_011516476.1:p.Arg795=
XM_011518175.1:c.2775G=	XP_011516477.1:p.Arg925=
XM_011518176.1:c.1791G=	XP_011516478.1:p.Arg597=
XM_011518177.1:c.1785G=	XP_011516479.1:p.Arg595=
XM_011518178.1:c.1440G=	XP_011516480.1:p.Arg480=
XM_011518179.1:c.1440G=	XP_011516481.1:p.Arg480=
XM_011518180.1:c.1041G=	XP_011516482.1:p.Arg347=
XM_011518176.3:c.1791G=	XP_011516478.1:p.Arg597=
XM_011518178.2:c.1440G=	XP_011516480.1:p.Arg480=
XM_017014232.1:c.2763G=	XP_016869721.1:p.Arg921=
XM_017014233.1:c.2385G=	XP_016869722.1:p.Arg795=
XM_017014234.2:c.1785G=	XP_016869723.1:p.Arg595=
XR_001746171.1:n.3548G=
NM_139026.5:c.2682G=	NP_620595.1:p.Arg894=
NM_139027.5:c.2775G=	NP_620596.2:p.Arg925=
NM_139025.5:c.2775G=	NP_620594.1:p.Arg925=
NM_139026.6:c.2682G=	NP_620595.1:p.Arg894=
NM_139027.6:c.2775G= MANE Select	NP_620596.2:p.Arg925=
NR_024514.3:n.1612G=