Canonical Allele Identifier: CA2284425249
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705399A= , CM000680.2:g.10705399A= GRCh38
NC_000018.9:g.10705397A= , CM000680.1:g.10705397A= GRCh37
NC_000018.8:g.10695397A= NCBI36
NG_034005.1:g.448364T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5672T= ENSP00000372900.4:p.Leu1891=
ENST00000643712.1:c.680T= ENSP00000493635.1:p.Leu227=
ENST00000674853.1:c.5936T= MANE Select ENSP00000501957.1:p.Leu1979=
ENST00000302079.10:c.5597T= ENSP00000303316.6:p.Leu1866=
ENST00000383408.6:c.5450T= ENSP00000372900.3:p.Leu1817=
ENST00000503781.7:c.5597T= ENSP00000421377.3:p.Leu1866=
ENST00000580640.5:c.5672T= ENSP00000463094.1:p.Leu1891=
ENST00000582913.5:c.5803T= ENSP00000462115.1:n.5803T=
NM_022068.3:c.5597T= NP_071351.2:p.Leu1866=
XM_011525723.1:c.5729T= XP_011524025.1:p.Leu1910=
XM_011525724.1:c.5672T= XP_011524026.1:p.Leu1891=
XM_011525725.1:c.5639T= XP_011524027.1:p.Leu1880=
XM_011525726.1:c.5729T= XP_011524028.1:p.Leu1910=
XM_011525723.3:c.5729T= XP_011524025.1:p.Leu1910=
XM_011525724.3:c.5672T= XP_011524026.1:p.Leu1891=
XM_011525725.3:c.5639T= XP_011524027.1:p.Leu1880=
XM_011525726.3:c.5729T= XP_011524028.1:p.Leu1910=
XM_017025918.2:c.5690T= XP_016881407.1:p.Leu1897=
XR_001753259.2:n.6726T=
NM_001378183.1:c.5936T= MANE Select NP_001365112.1:p.Leu1979=
NM_022068.4:c.5597T= NP_071351.2:p.Leu1866=