Canonical Allele Identifier: CA503243193

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10705384G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705386G>T , CM000680.2:g.10705386G>T	GRCh38
NC_000018.9:g.10705384G>T , CM000680.1:g.10705384G>T	GRCh37
NC_000018.8:g.10695384G>T	NCBI36
NG_034005.1:g.448377C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.5685C>A	ENSP00000372900.4:p.Ile1895=
ENST00000643712.1:c.693C>A	ENSP00000493635.1:p.Ile231=
ENST00000674853.1:c.5949C>A MANE Select	ENSP00000501957.1:p.Ile1983=
ENST00000302079.10:c.5610C>A	ENSP00000303316.6:p.Ile1870=
ENST00000383408.6:c.5463C>A	ENSP00000372900.3:p.Ile1821=
ENST00000503781.7:c.5610C>A	ENSP00000421377.3:p.Ile1870=
ENST00000580640.5:c.5685C>A	ENSP00000463094.1:p.Ile1895=
ENST00000582913.5:c.5816C>A	ENSP00000462115.1:n.5816C>A
NM_022068.3:c.5610C>A	NP_071351.2:p.Ile1870=
XM_011525723.1:c.5742C>A	XP_011524025.1:p.Ile1914=
XM_011525724.1:c.5685C>A	XP_011524026.1:p.Ile1895=
XM_011525725.1:c.5652C>A	XP_011524027.1:p.Ile1884=
XM_011525726.1:c.5742C>A	XP_011524028.1:p.Ile1914=
XM_011525723.3:c.5742C>A	XP_011524025.1:p.Ile1914=
XM_011525724.3:c.5685C>A	XP_011524026.1:p.Ile1895=
XM_011525725.3:c.5652C>A	XP_011524027.1:p.Ile1884=
XM_011525726.3:c.5742C>A	XP_011524028.1:p.Ile1914=
XM_017025918.2:c.5703C>A	XP_016881407.1:p.Ile1901=
XR_001753259.2:n.6739C>A
NM_001378183.1:c.5949C>A MANE Select	NP_001365112.1:p.Ile1983=
NM_022068.4:c.5610C>A	NP_071351.2:p.Ile1870=