Canonical Allele Identifier: CA503243143
Gene: PIEZO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.10705347G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705349G>A , CM000680.2:g.10705349G>A GRCh38
NC_000018.9:g.10705347G>A , CM000680.1:g.10705347G>A GRCh37
NC_000018.8:g.10695347G>A NCBI36
NG_034005.1:g.448414C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5722C>T ENSP00000372900.4:p.Leu1908=
ENST00000643712.1:c.730C>T ENSP00000493635.1:p.Leu244=
ENST00000674853.1:c.5986C>T MANE Select ENSP00000501957.1:p.Leu1996=
ENST00000302079.10:c.5647C>T ENSP00000303316.6:p.Leu1883=
ENST00000383408.6:c.5500C>T ENSP00000372900.3:p.Leu1834=
ENST00000503781.7:c.5647C>T ENSP00000421377.3:p.Leu1883=
ENST00000580640.5:c.5722C>T ENSP00000463094.1:p.Leu1908=
ENST00000582913.5:c.5853C>T ENSP00000462115.1:n.5853C>T
NM_022068.3:c.5647C>T NP_071351.2:p.Leu1883=
XM_011525723.1:c.5779C>T XP_011524025.1:p.Leu1927=
XM_011525724.1:c.5722C>T XP_011524026.1:p.Leu1908=
XM_011525725.1:c.5689C>T XP_011524027.1:p.Leu1897=
XM_011525726.1:c.5779C>T XP_011524028.1:p.Leu1927=
XM_011525723.3:c.5779C>T XP_011524025.1:p.Leu1927=
XM_011525724.3:c.5722C>T XP_011524026.1:p.Leu1908=
XM_011525725.3:c.5689C>T XP_011524027.1:p.Leu1897=
XM_011525726.3:c.5779C>T XP_011524028.1:p.Leu1927=
XM_017025918.2:c.5740C>T XP_016881407.1:p.Leu1914=
XR_001753259.2:n.6776C>T
NM_001378183.1:c.5986C>T MANE Select NP_001365112.1:p.Leu1996=
NM_022068.4:c.5647C>T NP_071351.2:p.Leu1883=