Canonical Allele Identifier: CA401910321
Gene: PIEZO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705391T>A , CM000680.2:g.10705391T>A GRCh38
NC_000018.9:g.10705389T>A , CM000680.1:g.10705389T>A GRCh37
NC_000018.8:g.10695389T>A NCBI36
NG_034005.1:g.448372A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5680A>T ENSP00000372900.4:p.Ser1894Cys
ENST00000643712.1:c.688A>T ENSP00000493635.1:p.Ser230Cys
ENST00000674853.1:c.5944A>T MANE Select ENSP00000501957.1:p.Ser1982Cys
ENST00000302079.10:c.5605A>T ENSP00000303316.6:p.Ser1869Cys
ENST00000383408.6:c.5458A>T ENSP00000372900.3:p.Ser1820Cys
ENST00000503781.7:c.5605A>T ENSP00000421377.3:p.Ser1869Cys
ENST00000580640.5:c.5680A>T ENSP00000463094.1:p.Ser1894Cys
ENST00000582913.5:c.5811A>T ENSP00000462115.1:n.5811A>T
NM_022068.3:c.5605A>T NP_071351.2:p.Ser1869Cys
XM_011525723.1:c.5737A>T XP_011524025.1:p.Ser1913Cys
XM_011525724.1:c.5680A>T XP_011524026.1:p.Ser1894Cys
XM_011525725.1:c.5647A>T XP_011524027.1:p.Ser1883Cys
XM_011525726.1:c.5737A>T XP_011524028.1:p.Ser1913Cys
XM_011525723.3:c.5737A>T XP_011524025.1:p.Ser1913Cys
XM_011525724.3:c.5680A>T XP_011524026.1:p.Ser1894Cys
XM_011525725.3:c.5647A>T XP_011524027.1:p.Ser1883Cys
XM_011525726.3:c.5737A>T XP_011524028.1:p.Ser1913Cys
XM_017025918.2:c.5698A>T XP_016881407.1:p.Ser1900Cys
XR_001753259.2:n.6734A>T
NM_001378183.1:c.5944A>T MANE Select NP_001365112.1:p.Ser1982Cys
NM_022068.4:c.5605A>T NP_071351.2:p.Ser1869Cys