Canonical Allele Identifier: CA375410212

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454472A>C , CM000671.2:g.133454472A>C	GRCh38
NC_000009.10:g.135309415A>C	NCBI36
NG_011934.2:g.45134A>C , LRG_544:g.45134A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.3102A>C MANE Select	ENSP00000347927.2:p.Arg1034Ser
ENST00000355699.6:c.3102A>C	ENSP00000347927.2:p.Arg1034Ser
ENST00000356589.6:c.3009A>C	ENSP00000348997.2:p.Arg1003Ser
ENST00000371916.5:c.*571A>C	ENSP00000360984.2:n.*571A>C
ENST00000371929.7:c.3102A>C	ENSP00000360997.3:p.Arg1034Ser
ENST00000485925.5:n.1918A>C
NM_139025.4:c.3102A>C , LRG_544t1:c.3102A>C	NP_620594.1:p.Arg1034Ser
NM_139026.4:c.3009A>C	NP_620595.1:p.Arg1003Ser
NM_139027.4:c.3102A>C	NP_620596.2:p.Arg1034Ser
NR_024514.2:n.1937A>C
XM_011518174.1:c.2712A>C	XP_011516476.1:p.Arg904Ser
XM_011518175.1:c.3102A>C	XP_011516477.1:p.Arg1034Ser
XM_011518176.1:c.2118A>C	XP_011516478.1:p.Arg706Ser
XM_011518177.1:c.2112A>C	XP_011516479.1:p.Arg704Ser
XM_011518178.1:c.1767A>C	XP_011516480.1:p.Arg589Ser
XM_011518179.1:c.1767A>C	XP_011516481.1:p.Arg589Ser
XM_011518180.1:c.1368A>C	XP_011516482.1:p.Arg456Ser
XM_011518176.3:c.2118A>C	XP_011516478.1:p.Arg706Ser
XM_011518178.2:c.1767A>C	XP_011516480.1:p.Arg589Ser
XM_017014232.1:c.3090A>C	XP_016869721.1:p.Arg1030Ser
XM_017014233.1:c.2712A>C	XP_016869722.1:p.Arg904Ser
XM_017014234.2:c.2112A>C	XP_016869723.1:p.Arg704Ser
NM_139026.5:c.3009A>C	NP_620595.1:p.Arg1003Ser
NM_139027.5:c.3102A>C	NP_620596.2:p.Arg1034Ser
NM_139025.5:c.3102A>C	NP_620594.1:p.Arg1034Ser
NM_139026.6:c.3009A>C	NP_620595.1:p.Arg1003Ser
NM_139027.6:c.3102A>C MANE Select	NP_620596.2:p.Arg1034Ser
NR_024514.3:n.1939A>C