Canonical Allele Identifier: CA375409985

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454426T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454426T>G , CM000671.2:g.133454426T>G	GRCh38
NC_000009.10:g.135309369T>G	NCBI36
NG_011934.2:g.45088T>G , LRG_544:g.45088T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3056T>G MANE Select	ENSP00000347927.2:p.Met1019Arg
ENST00000355699.6:c.3056T>G	ENSP00000347927.2:p.Met1019Arg
ENST00000356589.6:c.2963T>G	ENSP00000348997.2:p.Met988Arg
ENST00000371916.5:c.*525T>G	ENSP00000360984.2:n.*525T>G
ENST00000371929.7:c.3056T>G	ENSP00000360997.3:p.Met1019Arg
ENST00000485925.5:n.1872T>G
NM_139025.4:c.3056T>G , LRG_544t1:c.3056T>G	NP_620594.1:p.Met1019Arg
NM_139026.4:c.2963T>G	NP_620595.1:p.Met988Arg
NM_139027.4:c.3056T>G	NP_620596.2:p.Met1019Arg
NR_024514.2:n.1891T>G
XM_011518174.1:c.2666T>G	XP_011516476.1:p.Met889Arg
XM_011518175.1:c.3056T>G	XP_011516477.1:p.Met1019Arg
XM_011518176.1:c.2072T>G	XP_011516478.1:p.Met691Arg
XM_011518177.1:c.2066T>G	XP_011516479.1:p.Met689Arg
XM_011518178.1:c.1721T>G	XP_011516480.1:p.Met574Arg
XM_011518179.1:c.1721T>G	XP_011516481.1:p.Met574Arg
XM_011518180.1:c.1322T>G	XP_011516482.1:p.Met441Arg
XM_011518176.3:c.2072T>G	XP_011516478.1:p.Met691Arg
XM_011518178.2:c.1721T>G	XP_011516480.1:p.Met574Arg
XM_017014232.1:c.3044T>G	XP_016869721.1:p.Met1015Arg
XM_017014233.1:c.2666T>G	XP_016869722.1:p.Met889Arg
XM_017014234.2:c.2066T>G	XP_016869723.1:p.Met689Arg
XR_001746171.1:n.3829T>G
NM_139026.5:c.2963T>G	NP_620595.1:p.Met988Arg
NM_139027.5:c.3056T>G	NP_620596.2:p.Met1019Arg
NM_139025.5:c.3056T>G	NP_620594.1:p.Met1019Arg
NM_139026.6:c.2963T>G	NP_620595.1:p.Met988Arg
NM_139027.6:c.3056T>G MANE Select	NP_620596.2:p.Met1019Arg
NR_024514.3:n.1893T>G