Canonical Allele Identifier: CA375409979

Gene: ADAMTS13

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3056T>A MANE Select	ENSP00000347927.2:p.Met1019Lys
ENST00000355699.6:c.3056T>A	ENSP00000347927.2:p.Met1019Lys
ENST00000356589.6:c.2963T>A	ENSP00000348997.2:p.Met988Lys
ENST00000371916.5:c.*525T>A	ENSP00000360984.2:n.*525T>A
ENST00000371929.7:c.3056T>A	ENSP00000360997.3:p.Met1019Lys
ENST00000485925.5:n.1872T>A
NM_139025.4:c.3056T>A , LRG_544t1:c.3056T>A	NP_620594.1:p.Met1019Lys
NM_139026.4:c.2963T>A	NP_620595.1:p.Met988Lys
NM_139027.4:c.3056T>A	NP_620596.2:p.Met1019Lys
NR_024514.2:n.1891T>A
XM_011518174.1:c.2666T>A	XP_011516476.1:p.Met889Lys
XM_011518175.1:c.3056T>A	XP_011516477.1:p.Met1019Lys
XM_011518176.1:c.2072T>A	XP_011516478.1:p.Met691Lys
XM_011518177.1:c.2066T>A	XP_011516479.1:p.Met689Lys
XM_011518178.1:c.1721T>A	XP_011516480.1:p.Met574Lys
XM_011518179.1:c.1721T>A	XP_011516481.1:p.Met574Lys
XM_011518180.1:c.1322T>A	XP_011516482.1:p.Met441Lys
XM_011518176.3:c.2072T>A	XP_011516478.1:p.Met691Lys
XM_011518178.2:c.1721T>A	XP_011516480.1:p.Met574Lys
XM_017014232.1:c.3044T>A	XP_016869721.1:p.Met1015Lys
XM_017014233.1:c.2666T>A	XP_016869722.1:p.Met889Lys
XM_017014234.2:c.2066T>A	XP_016869723.1:p.Met689Lys
XR_001746171.1:n.3829T>A
NM_139026.5:c.2963T>A	NP_620595.1:p.Met988Lys
NM_139027.5:c.3056T>A	NP_620596.2:p.Met1019Lys
NM_139025.5:c.3056T>A	NP_620594.1:p.Met1019Lys
NM_139026.6:c.2963T>A	NP_620595.1:p.Met988Lys
NM_139027.6:c.3056T>A MANE Select	NP_620596.2:p.Met1019Lys
NR_024514.3:n.1893T>A