Canonical Allele Identifier: CA1882682405

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133456039_133456040delinsCT , CM000671.2:g.133456039_133456040delinsCT	GRCh38
NC_000009.10:g.135310982_135310983delinsCT	NCBI36
NG_011934.2:g.46701_46702delinsCT , LRG_544:g.46701_46702delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3401-30_3401-29delinsCT MANE Select	ENSP00000347927.2:n.3401-30_3401-29delinsCT
ENST00000355699.6:c.3401-30_3401-29delinsCT	ENSP00000347927.2:n.3401-30_3401-29delinsCT
ENST00000356589.6:c.3308-30_3308-29delinsCT	ENSP00000348997.2:n.3308-30_3308-29delinsCT
ENST00000371910.1:c.-44-30_-44-29delinsCT	ENSP00000360978.1:n.-44-30_-44-29delinsCT
ENST00000371916.5:c.*870-30_*870-29delinsCT	ENSP00000360984.2:n.*870-30_*870-29delinsCT
ENST00000371929.7:c.3569-30_3569-29delinsCT	ENSP00000360997.3:n.3569-30_3569-29delinsCT
ENST00000485925.5:n.2217-30_2217-29delinsCT
NM_139025.4:c.3569-30_3569-29delinsCT , LRG_544t1:c.3569-30_3569-29delinsCT	NP_620594.1:n.3569-30_3569-29delinsCT
NM_139026.4:c.3308-30_3308-29delinsCT	NP_620595.1:n.3308-30_3308-29delinsCT
NM_139027.4:c.3401-30_3401-29delinsCT	NP_620596.2:n.3401-30_3401-29delinsCT
NR_024514.2:n.2236-30_2236-29delinsCT
XM_011518174.1:c.3179-30_3179-29delinsCT	XP_011516476.1:n.3179-30_3179-29delinsCT
XM_011518175.1:c.3570-30_3570-29delinsCT	XP_011516477.1:n.3570-30_3570-29delinsCT
XM_011518176.1:c.2585-30_2585-29delinsCT	XP_011516478.1:n.2585-30_2585-29delinsCT
XM_011518177.1:c.2579-30_2579-29delinsCT	XP_011516479.1:n.2579-30_2579-29delinsCT
XM_011518178.1:c.2234-30_2234-29delinsCT	XP_011516480.1:n.2234-30_2234-29delinsCT
XM_011518179.1:c.2234-30_2234-29delinsCT	XP_011516481.1:n.2234-30_2234-29delinsCT
XM_011518180.1:c.1835-30_1835-29delinsCT	XP_011516482.1:n.1835-30_1835-29delinsCT
XM_011518176.3:c.2585-30_2585-29delinsCT	XP_011516478.1:n.2585-30_2585-29delinsCT
XM_011518178.2:c.2234-30_2234-29delinsCT	XP_011516480.1:n.2234-30_2234-29delinsCT
XM_017014232.1:c.3557-30_3557-29delinsCT	XP_016869721.1:n.3557-30_3557-29delinsCT
XM_017014233.1:c.3179-30_3179-29delinsCT	XP_016869722.1:n.3179-30_3179-29delinsCT
XM_017014234.2:c.2579-30_2579-29delinsCT	XP_016869723.1:n.2579-30_2579-29delinsCT
NM_139026.5:c.3308-30_3308-29delinsCT	NP_620595.1:n.3308-30_3308-29delinsCT
NM_139027.5:c.3401-30_3401-29delinsCT	NP_620596.2:n.3401-30_3401-29delinsCT
NM_139025.5:c.3569-30_3569-29delinsCT	NP_620594.1:n.3569-30_3569-29delinsCT
NM_139026.6:c.3308-30_3308-29delinsCT	NP_620595.1:n.3308-30_3308-29delinsCT
NM_139027.6:c.3401-30_3401-29delinsCT MANE Select	NP_620596.2:n.3401-30_3401-29delinsCT
NR_024514.3:n.2238-30_2238-29delinsCT