Canonical Allele Identifier: CA375391603

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133436875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436875G>C , CM000671.2:g.133436875G>C	GRCh38
NC_000009.10:g.135291816G>C	NCBI36
NG_011934.2:g.27537G>C , LRG_544:g.27537G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.1355G>C MANE Select	ENSP00000347927.2:p.Arg452Thr
ENST00000355699.6:c.1355G>C	ENSP00000347927.2:p.Arg452Thr
ENST00000356589.6:c.1262G>C	ENSP00000348997.2:p.Arg421Thr
ENST00000371916.5:c.611G>C	ENSP00000360984.2:p.Arg204Thr
ENST00000371929.7:c.1355G>C	ENSP00000360997.3:p.Arg452Thr
ENST00000474918.1:c.*159G>C	ENSP00000435305.1:n.*159G>C
ENST00000485925.5:n.974-2491G>C
ENST00000495234.5:c.*639G>C	ENSP00000435274.1:n.*639G>C
NM_139025.4:c.1355G>C , LRG_544t1:c.1355G>C	NP_620594.1:p.Arg452Thr
NM_139026.4:c.1262G>C	NP_620595.1:p.Arg421Thr
NM_139027.4:c.1355G>C	NP_620596.2:p.Arg452Thr
NR_024514.2:n.993-2491G>C
XM_011518174.1:c.965G>C	XP_011516476.1:p.Arg322Thr
XM_011518175.1:c.1355G>C	XP_011516477.1:p.Arg452Thr
XM_011518176.1:c.371G>C	XP_011516478.1:p.Arg124Thr
XM_011518177.1:c.365G>C	XP_011516479.1:p.Arg122Thr
XM_011518178.1:c.20G>C	XP_011516480.1:p.Arg7Thr
XM_011518179.1:c.141G>C	XP_011516481.1:p.Gln47His
XM_011518180.1:c.687-7988G>C	XP_011516482.1:n.687-7988G>C
XM_011518176.3:c.371G>C	XP_011516478.1:p.Arg124Thr
XM_011518178.2:c.20G>C	XP_011516480.1:p.Arg7Thr
XM_017014232.1:c.1343G>C	XP_016869721.1:p.Arg448Thr
XM_017014233.1:c.965G>C	XP_016869722.1:p.Arg322Thr
XM_017014234.2:c.365G>C	XP_016869723.1:p.Arg122Thr
XM_017014235.1:c.1355G>C	XP_016869724.1:p.Arg452Thr
XR_001746171.1:n.2580G>C
NM_139026.5:c.1262G>C	NP_620595.1:p.Arg421Thr
NM_139027.5:c.1355G>C	NP_620596.2:p.Arg452Thr
NM_139025.5:c.1355G>C	NP_620594.1:p.Arg452Thr
NM_139026.6:c.1262G>C	NP_620595.1:p.Arg421Thr
NM_139027.6:c.1355G>C MANE Select	NP_620596.2:p.Arg452Thr
NR_024514.3:n.995-2491G>C