Canonical Allele Identifier: CA503243204

Gene: PIEZO2

Linked Data

• gnomAD v4: 18-10705395-C-A
• MyVariant Identifiers: chr18:g.10705393C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705395C>A , CM000680.2:g.10705395C>A	GRCh38
NC_000018.9:g.10705393C>A , CM000680.1:g.10705393C>A	GRCh37
NC_000018.8:g.10695393C>A	NCBI36
NG_034005.1:g.448368G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.5676G>T	ENSP00000372900.4:p.Gly1892=
ENST00000643712.1:c.684G>T	ENSP00000493635.1:p.Gly228=
ENST00000674853.1:c.5940G>T MANE Select	ENSP00000501957.1:p.Gly1980=
ENST00000302079.10:c.5601G>T	ENSP00000303316.6:p.Gly1867=
ENST00000383408.6:c.5454G>T	ENSP00000372900.3:p.Gly1818=
ENST00000503781.7:c.5601G>T	ENSP00000421377.3:p.Gly1867=
ENST00000580640.5:c.5676G>T	ENSP00000463094.1:p.Gly1892=
ENST00000582913.5:c.5807G>T	ENSP00000462115.1:n.5807G>T
NM_022068.3:c.5601G>T	NP_071351.2:p.Gly1867=
XM_011525723.1:c.5733G>T	XP_011524025.1:p.Gly1911=
XM_011525724.1:c.5676G>T	XP_011524026.1:p.Gly1892=
XM_011525725.1:c.5643G>T	XP_011524027.1:p.Gly1881=
XM_011525726.1:c.5733G>T	XP_011524028.1:p.Gly1911=
XM_011525723.3:c.5733G>T	XP_011524025.1:p.Gly1911=
XM_011525724.3:c.5676G>T	XP_011524026.1:p.Gly1892=
XM_011525725.3:c.5643G>T	XP_011524027.1:p.Gly1881=
XM_011525726.3:c.5733G>T	XP_011524028.1:p.Gly1911=
XM_017025918.2:c.5694G>T	XP_016881407.1:p.Gly1898=
XR_001753259.2:n.6730G>T
NM_001378183.1:c.5940G>T MANE Select	NP_001365112.1:p.Gly1980=
NM_022068.4:c.5601G>T	NP_071351.2:p.Gly1867=