Canonical Allele Identifier: CA375404295

Gene: ADAMTS13

Linked Data

• dbSNP Id: rs1554793326
• gnomAD v4: 9-133448686-G-C
• MyVariant Identifiers: chr9:g.133448686G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133448686G>C , CM000671.2:g.133448686G>C	GRCh38
NC_000009.10:g.135303628G>C	NCBI36
NG_011934.2:g.39348G>C , LRG_544:g.39348G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2819G>C MANE Select	ENSP00000347927.2:p.Gly940Ala
ENST00000355699.6:c.2819G>C	ENSP00000347927.2:p.Gly940Ala
ENST00000356589.6:c.2726G>C	ENSP00000348997.2:p.Gly909Ala
ENST00000371916.5:c.*288G>C	ENSP00000360984.2:n.*288G>C
ENST00000371929.7:c.2819G>C	ENSP00000360997.3:p.Gly940Ala
ENST00000485925.5:n.1635G>C
ENST00000495234.5:c.*1651G>C	ENSP00000435274.1:n.*1651G>C
NM_139025.4:c.2819G>C , LRG_544t1:c.2819G>C	NP_620594.1:p.Gly940Ala
NM_139026.4:c.2726G>C	NP_620595.1:p.Gly909Ala
NM_139027.4:c.2819G>C	NP_620596.2:p.Gly940Ala
NR_024514.2:n.1654G>C
XM_011518174.1:c.2429G>C	XP_011516476.1:p.Gly810Ala
XM_011518175.1:c.2819G>C	XP_011516477.1:p.Gly940Ala
XM_011518176.1:c.1835G>C	XP_011516478.1:p.Gly612Ala
XM_011518177.1:c.1829G>C	XP_011516479.1:p.Gly610Ala
XM_011518178.1:c.1484G>C	XP_011516480.1:p.Gly495Ala
XM_011518179.1:c.1484G>C	XP_011516481.1:p.Gly495Ala
XM_011518180.1:c.1085G>C	XP_011516482.1:p.Gly362Ala
XM_011518176.3:c.1835G>C	XP_011516478.1:p.Gly612Ala
XM_011518178.2:c.1484G>C	XP_011516480.1:p.Gly495Ala
XM_017014232.1:c.2807G>C	XP_016869721.1:p.Gly936Ala
XM_017014233.1:c.2429G>C	XP_016869722.1:p.Gly810Ala
XM_017014234.2:c.1829G>C	XP_016869723.1:p.Gly610Ala
XR_001746171.1:n.3592G>C
NM_139026.5:c.2726G>C	NP_620595.1:p.Gly909Ala
NM_139027.5:c.2819G>C	NP_620596.2:p.Gly940Ala
NM_139025.5:c.2819G>C	NP_620594.1:p.Gly940Ala
NM_139026.6:c.2726G>C	NP_620595.1:p.Gly909Ala
NM_139027.6:c.2819G>C MANE Select	NP_620596.2:p.Gly940Ala
NR_024514.3:n.1656G>C