Canonical Allele Identifier: CA1882682448

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133456126G= , CM000671.2:g.133456126G=	GRCh38
NC_000009.10:g.135311069G=	NCBI36
NG_011934.2:g.46788G= , LRG_544:g.46788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3458G= MANE Select	ENSP00000347927.2:p.Gly1153=
ENST00000355699.6:c.3458G=	ENSP00000347927.2:p.Gly1153=
ENST00000356589.6:c.3365G=	ENSP00000348997.2:p.Gly1122=
ENST00000371910.1:c.14G=	ENSP00000360978.1:p.Gly5=
ENST00000371916.5:c.*927G=	ENSP00000360984.2:n.*927G=
ENST00000371929.7:c.3626G=	ENSP00000360997.3:p.Gly1209=
ENST00000485925.5:n.2274G=
NM_139025.4:c.3626G= , LRG_544t1:c.3626G=	NP_620594.1:p.Gly1209=
NM_139026.4:c.3365G=	NP_620595.1:p.Gly1122=
NM_139027.4:c.3458G=	NP_620596.2:p.Gly1153=
NR_024514.2:n.2293G=
XM_011518174.1:c.3236G=	XP_011516476.1:p.Gly1079=
XM_011518175.1:c.*33G=	XP_011516477.1:n.*33G=
XM_011518176.1:c.2642G=	XP_011516478.1:p.Gly881=
XM_011518177.1:c.2636G=	XP_011516479.1:p.Gly879=
XM_011518178.1:c.2291G=	XP_011516480.1:p.Gly764=
XM_011518179.1:c.2291G=	XP_011516481.1:p.Gly764=
XM_011518180.1:c.1892G=	XP_011516482.1:p.Gly631=
XM_011518176.3:c.2642G=	XP_011516478.1:p.Gly881=
XM_011518178.2:c.2291G=	XP_011516480.1:p.Gly764=
XM_017014232.1:c.3614G=	XP_016869721.1:p.Gly1205=
XM_017014233.1:c.3236G=	XP_016869722.1:p.Gly1079=
XM_017014234.2:c.2636G=	XP_016869723.1:p.Gly879=
NM_139026.5:c.3365G=	NP_620595.1:p.Gly1122=
NM_139027.5:c.3458G=	NP_620596.2:p.Gly1153=
NM_139025.5:c.3626G=	NP_620594.1:p.Gly1209=
NM_139026.6:c.3365G=	NP_620595.1:p.Gly1122=
NM_139027.6:c.3458G= MANE Select	NP_620596.2:p.Gly1153=
NR_024514.3:n.2295G=