Canonical Allele Identifier: CA375391644

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133436884G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436884G>C , CM000671.2:g.133436884G>C	GRCh38
NC_000009.10:g.135291825G>C	NCBI36
NG_011934.2:g.27546G>C , LRG_544:g.27546G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1364G>C MANE Select	ENSP00000347927.2:p.Gly455Ala
ENST00000355699.6:c.1364G>C	ENSP00000347927.2:p.Gly455Ala
ENST00000356589.6:c.1271G>C	ENSP00000348997.2:p.Gly424Ala
ENST00000371916.5:c.620G>C	ENSP00000360984.2:p.Gly207Ala
ENST00000371929.7:c.1364G>C	ENSP00000360997.3:p.Gly455Ala
ENST00000474918.1:c.*168G>C	ENSP00000435305.1:n.*168G>C
ENST00000485925.5:n.974-2482G>C
ENST00000495234.5:c.*648G>C	ENSP00000435274.1:n.*648G>C
NM_139025.4:c.1364G>C , LRG_544t1:c.1364G>C	NP_620594.1:p.Gly455Ala
NM_139026.4:c.1271G>C	NP_620595.1:p.Gly424Ala
NM_139027.4:c.1364G>C	NP_620596.2:p.Gly455Ala
NR_024514.2:n.993-2482G>C
XM_011518174.1:c.974G>C	XP_011516476.1:p.Gly325Ala
XM_011518175.1:c.1364G>C	XP_011516477.1:p.Gly455Ala
XM_011518176.1:c.380G>C	XP_011516478.1:p.Gly127Ala
XM_011518177.1:c.374G>C	XP_011516479.1:p.Gly125Ala
XM_011518178.1:c.29G>C	XP_011516480.1:p.Gly10Ala
XM_011518179.1:c.150G>C	XP_011516481.1:p.Arg50=
XM_011518180.1:c.687-7979G>C	XP_011516482.1:n.687-7979G>C
XM_011518176.3:c.380G>C	XP_011516478.1:p.Gly127Ala
XM_011518178.2:c.29G>C	XP_011516480.1:p.Gly10Ala
XM_017014232.1:c.1352G>C	XP_016869721.1:p.Gly451Ala
XM_017014233.1:c.974G>C	XP_016869722.1:p.Gly325Ala
XM_017014234.2:c.374G>C	XP_016869723.1:p.Gly125Ala
XM_017014235.1:c.1364G>C	XP_016869724.1:p.Gly455Ala
XR_001746171.1:n.2589G>C
NM_139026.5:c.1271G>C	NP_620595.1:p.Gly424Ala
NM_139027.5:c.1364G>C	NP_620596.2:p.Gly455Ala
NM_139025.5:c.1364G>C	NP_620594.1:p.Gly455Ala
NM_139026.6:c.1271G>C	NP_620595.1:p.Gly424Ala
NM_139027.6:c.1364G>C MANE Select	NP_620596.2:p.Gly455Ala
NR_024514.3:n.995-2482G>C