Canonical Allele Identifier: CA375405103

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133449781-A-C
• MyVariant Identifiers: chr9:g.133449781A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133449781A>C , CM000671.2:g.133449781A>C	GRCh38
NC_000009.10:g.135304723A>C	NCBI36
NG_011934.2:g.40443A>C , LRG_544:g.40443A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2862-2A>C MANE Select	ENSP00000347927.2:n.2862-2A>C
ENST00000355699.6:c.2862-2A>C	ENSP00000347927.2:n.2862-2A>C
ENST00000356589.6:c.2769-2A>C	ENSP00000348997.2:n.2769-2A>C
ENST00000371916.5:c.*331-2A>C	ENSP00000360984.2:n.*331-2A>C
ENST00000371929.7:c.2862-2A>C	ENSP00000360997.3:n.2862-2A>C
ENST00000485925.5:n.1678-2A>C
ENST00000495234.5:c.*1694-2A>C	ENSP00000435274.1:n.*1694-2A>C
NM_139025.4:c.2862-2A>C , LRG_544t1:c.2862-2A>C	NP_620594.1:n.2862-2A>C
NM_139026.4:c.2769-2A>C	NP_620595.1:n.2769-2A>C
NM_139027.4:c.2862-2A>C	NP_620596.2:n.2862-2A>C
NR_024514.2:n.1697-2A>C
XM_011518174.1:c.2472-2A>C	XP_011516476.1:n.2472-2A>C
XM_011518175.1:c.2862-2A>C	XP_011516477.1:n.2862-2A>C
XM_011518176.1:c.1878-2A>C	XP_011516478.1:n.1878-2A>C
XM_011518177.1:c.1872-2A>C	XP_011516479.1:n.1872-2A>C
XM_011518178.1:c.1527-2A>C	XP_011516480.1:n.1527-2A>C
XM_011518179.1:c.1527-2A>C	XP_011516481.1:n.1527-2A>C
XM_011518180.1:c.1128-2A>C	XP_011516482.1:n.1128-2A>C
XM_011518176.3:c.1878-2A>C	XP_011516478.1:n.1878-2A>C
XM_011518178.2:c.1527-2A>C	XP_011516480.1:n.1527-2A>C
XM_017014232.1:c.2850-2A>C	XP_016869721.1:n.2850-2A>C
XM_017014233.1:c.2472-2A>C	XP_016869722.1:n.2472-2A>C
XM_017014234.2:c.1872-2A>C	XP_016869723.1:n.1872-2A>C
XR_001746171.1:n.3635-2A>C
NM_139026.5:c.2769-2A>C	NP_620595.1:n.2769-2A>C
NM_139027.5:c.2862-2A>C	NP_620596.2:n.2862-2A>C
NM_139025.5:c.2862-2A>C	NP_620594.1:n.2862-2A>C
NM_139026.6:c.2769-2A>C	NP_620595.1:n.2769-2A>C
NM_139027.6:c.2862-2A>C MANE Select	NP_620596.2:n.2862-2A>C
NR_024514.3:n.1699-2A>C