Canonical Allele Identifier: CA10629426

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133449836G>A , CM000671.2:g.133449836G>A	GRCh38
NC_000009.10:g.135304778G>A	NCBI36
NG_011934.2:g.40498G>A , LRG_544:g.40498G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_139027.6:c.2915G>A MANE Select	NP_620596.2:p.Arg972Gln
ENST00000355699.7:c.2915G>A MANE Select	ENSP00000347927.2:p.Arg972Gln
NM_139025.4:c.2915G>A , LRG_544t1:c.2915G>A	NP_620594.1:p.Arg972Gln
NM_139025.5:c.2915G>A	NP_620594.1:p.Arg972Gln
NM_139026.4:c.2822G>A	NP_620595.1:p.Arg941Gln
NM_139026.5:c.2822G>A	NP_620595.1:p.Arg941Gln
NM_139026.6:c.2822G>A	NP_620595.1:p.Arg941Gln
NM_139027.4:c.2915G>A	NP_620596.2:p.Arg972Gln
NM_139027.5:c.2915G>A	NP_620596.2:p.Arg972Gln
NR_024514.2:n.1750G>A
NR_024514.3:n.1752G>A
ENST00000355699.6:c.2915G>A	ENSP00000347927.2:p.Arg972Gln
ENST00000356589.6:c.2822G>A	ENSP00000348997.2:p.Arg941Gln
ENST00000371916.5:c.*384G>A	ENSP00000360984.2:n.*384G>A
ENST00000371929.7:c.2915G>A	ENSP00000360997.3:p.Arg972Gln
ENST00000485925.5:n.1731G>A
ENST00000495234.5:c.*1747G>A	ENSP00000435274.1:n.*1747G>A
XM_011518174.1:c.2525G>A	XP_011516476.1:p.Arg842Gln
XM_011518175.1:c.2915G>A	XP_011516477.1:p.Arg972Gln
XM_011518176.1:c.1931G>A	XP_011516478.1:p.Arg644Gln
XM_011518176.3:c.1931G>A	XP_011516478.1:p.Arg644Gln
XM_011518177.1:c.1925G>A	XP_011516479.1:p.Arg642Gln
XM_011518178.1:c.1580G>A	XP_011516480.1:p.Arg527Gln
XM_011518178.2:c.1580G>A	XP_011516480.1:p.Arg527Gln
XM_011518179.1:c.1580G>A	XP_011516481.1:p.Arg527Gln
XM_011518180.1:c.1181G>A	XP_011516482.1:p.Arg394Gln
XM_017014232.1:c.2903G>A	XP_016869721.1:p.Arg968Gln
XM_017014233.1:c.2525G>A	XP_016869722.1:p.Arg842Gln
XM_017014234.2:c.1925G>A	XP_016869723.1:p.Arg642Gln
XR_001746171.1:n.3688G>A