Canonical Allele Identifier: CA375410056

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454435G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454435G>T , CM000671.2:g.133454435G>T	GRCh38
NC_000009.10:g.135309378G>T	NCBI36
NG_011934.2:g.45097G>T , LRG_544:g.45097G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3065G>T MANE Select	ENSP00000347927.2:p.Gly1022Val
ENST00000355699.6:c.3065G>T	ENSP00000347927.2:p.Gly1022Val
ENST00000356589.6:c.2972G>T	ENSP00000348997.2:p.Gly991Val
ENST00000371916.5:c.*534G>T	ENSP00000360984.2:n.*534G>T
ENST00000371929.7:c.3065G>T	ENSP00000360997.3:p.Gly1022Val
ENST00000485925.5:n.1881G>T
NM_139025.4:c.3065G>T , LRG_544t1:c.3065G>T	NP_620594.1:p.Gly1022Val
NM_139026.4:c.2972G>T	NP_620595.1:p.Gly991Val
NM_139027.4:c.3065G>T	NP_620596.2:p.Gly1022Val
NR_024514.2:n.1900G>T
XM_011518174.1:c.2675G>T	XP_011516476.1:p.Gly892Val
XM_011518175.1:c.3065G>T	XP_011516477.1:p.Gly1022Val
XM_011518176.1:c.2081G>T	XP_011516478.1:p.Gly694Val
XM_011518177.1:c.2075G>T	XP_011516479.1:p.Gly692Val
XM_011518178.1:c.1730G>T	XP_011516480.1:p.Gly577Val
XM_011518179.1:c.1730G>T	XP_011516481.1:p.Gly577Val
XM_011518180.1:c.1331G>T	XP_011516482.1:p.Gly444Val
XM_011518176.3:c.2081G>T	XP_011516478.1:p.Gly694Val
XM_011518178.2:c.1730G>T	XP_011516480.1:p.Gly577Val
XM_017014232.1:c.3053G>T	XP_016869721.1:p.Gly1018Val
XM_017014233.1:c.2675G>T	XP_016869722.1:p.Gly892Val
XM_017014234.2:c.2075G>T	XP_016869723.1:p.Gly692Val
XR_001746171.1:n.3838G>T
NM_139026.5:c.2972G>T	NP_620595.1:p.Gly991Val
NM_139027.5:c.3065G>T	NP_620596.2:p.Gly1022Val
NM_139025.5:c.3065G>T	NP_620594.1:p.Gly1022Val
NM_139026.6:c.2972G>T	NP_620595.1:p.Gly991Val
NM_139027.6:c.3065G>T MANE Select	NP_620596.2:p.Gly1022Val
NR_024514.3:n.1902G>T