Canonical Allele Identifier: CA375410126

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133454450-G-C
• MyVariant Identifiers: chr9:g.133454450G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454450G>C , CM000671.2:g.133454450G>C	GRCh38
NC_000009.10:g.135309393G>C	NCBI36
NG_011934.2:g.45112G>C , LRG_544:g.45112G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3080G>C MANE Select	ENSP00000347927.2:p.Ser1027Thr
ENST00000355699.6:c.3080G>C	ENSP00000347927.2:p.Ser1027Thr
ENST00000356589.6:c.2987G>C	ENSP00000348997.2:p.Ser996Thr
ENST00000371916.5:c.*549G>C	ENSP00000360984.2:n.*549G>C
ENST00000371929.7:c.3080G>C	ENSP00000360997.3:p.Ser1027Thr
ENST00000485925.5:n.1896G>C
NM_139025.4:c.3080G>C , LRG_544t1:c.3080G>C	NP_620594.1:p.Ser1027Thr
NM_139026.4:c.2987G>C	NP_620595.1:p.Ser996Thr
NM_139027.4:c.3080G>C	NP_620596.2:p.Ser1027Thr
NR_024514.2:n.1915G>C
XM_011518174.1:c.2690G>C	XP_011516476.1:p.Ser897Thr
XM_011518175.1:c.3080G>C	XP_011516477.1:p.Ser1027Thr
XM_011518176.1:c.2096G>C	XP_011516478.1:p.Ser699Thr
XM_011518177.1:c.2090G>C	XP_011516479.1:p.Ser697Thr
XM_011518178.1:c.1745G>C	XP_011516480.1:p.Ser582Thr
XM_011518179.1:c.1745G>C	XP_011516481.1:p.Ser582Thr
XM_011518180.1:c.1346G>C	XP_011516482.1:p.Ser449Thr
XM_011518176.3:c.2096G>C	XP_011516478.1:p.Ser699Thr
XM_011518178.2:c.1745G>C	XP_011516480.1:p.Ser582Thr
XM_017014232.1:c.3068G>C	XP_016869721.1:p.Ser1023Thr
XM_017014233.1:c.2690G>C	XP_016869722.1:p.Ser897Thr
XM_017014234.2:c.2090G>C	XP_016869723.1:p.Ser697Thr
XR_001746171.1:n.3853G>C
NM_139026.5:c.2987G>C	NP_620595.1:p.Ser996Thr
NM_139027.5:c.3080G>C	NP_620596.2:p.Ser1027Thr
NM_139025.5:c.3080G>C	NP_620594.1:p.Ser1027Thr
NM_139026.6:c.2987G>C	NP_620595.1:p.Ser996Thr
NM_139027.6:c.3080G>C MANE Select	NP_620596.2:p.Ser1027Thr
NR_024514.3:n.1917G>C