Canonical Allele Identifier: CA1882678620

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133449865G= , CM000671.2:g.133449865G=	GRCh38
NC_000009.10:g.135304807G=	NCBI36
NG_011934.2:g.40527G= , LRG_544:g.40527G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2944G= MANE Select	ENSP00000347927.2:p.Gly982=
ENST00000355699.6:c.2944G=	ENSP00000347927.2:p.Gly982=
ENST00000356589.6:c.2851G=	ENSP00000348997.2:p.Gly951=
ENST00000371916.5:c.*413G=	ENSP00000360984.2:n.*413G=
ENST00000371929.7:c.2944G=	ENSP00000360997.3:p.Gly982=
ENST00000485925.5:n.1760G=
ENST00000495234.5:c.*1776G=	ENSP00000435274.1:n.*1776G=
NM_139025.4:c.2944G= , LRG_544t1:c.2944G=	NP_620594.1:p.Gly982=
NM_139026.4:c.2851G=	NP_620595.1:p.Gly951=
NM_139027.4:c.2944G=	NP_620596.2:p.Gly982=
NR_024514.2:n.1779G=
XM_011518174.1:c.2554G=	XP_011516476.1:p.Gly852=
XM_011518175.1:c.2944G=	XP_011516477.1:p.Gly982=
XM_011518176.1:c.1960G=	XP_011516478.1:p.Gly654=
XM_011518177.1:c.1954G=	XP_011516479.1:p.Gly652=
XM_011518178.1:c.1609G=	XP_011516480.1:p.Gly537=
XM_011518179.1:c.1609G=	XP_011516481.1:p.Gly537=
XM_011518180.1:c.1210G=	XP_011516482.1:p.Gly404=
XM_011518176.3:c.1960G=	XP_011516478.1:p.Gly654=
XM_011518178.2:c.1609G=	XP_011516480.1:p.Gly537=
XM_017014232.1:c.2932G=	XP_016869721.1:p.Gly978=
XM_017014233.1:c.2554G=	XP_016869722.1:p.Gly852=
XM_017014234.2:c.1954G=	XP_016869723.1:p.Gly652=
XR_001746171.1:n.3717G=
NM_139026.5:c.2851G=	NP_620595.1:p.Gly951=
NM_139027.5:c.2944G=	NP_620596.2:p.Gly982=
NM_139025.5:c.2944G=	NP_620594.1:p.Gly982=
NM_139026.6:c.2851G=	NP_620595.1:p.Gly951=
NM_139027.6:c.2944G= MANE Select	NP_620596.2:p.Gly982=
NR_024514.3:n.1781G=