Canonical Allele Identifier: CA2284425246
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705389G= , CM000680.2:g.10705389G= GRCh38
NC_000018.9:g.10705387G= , CM000680.1:g.10705387G= GRCh37
NC_000018.8:g.10695387G= NCBI36
NG_034005.1:g.448374C=

Transcript Alleles

HGVS Amino-acid change
ENST00000383408.7:c.5682C= ENSP00000372900.4:p.Ser1894=
ENST00000643712.1:c.690C= ENSP00000493635.1:p.Ser230=
ENST00000674853.1:c.5946C= MANE Select ENSP00000501957.1:p.Ser1982=
ENST00000302079.10:c.5607C= ENSP00000303316.6:p.Ser1869=
ENST00000383408.6:c.5460C= ENSP00000372900.3:p.Ser1820=
ENST00000503781.7:c.5607C= ENSP00000421377.3:p.Ser1869=
ENST00000580640.5:c.5682C= ENSP00000463094.1:p.Ser1894=
ENST00000582913.5:c.5813C= ENSP00000462115.1:n.5813C=
NM_022068.3:c.5607C= NP_071351.2:p.Ser1869=
XM_011525723.1:c.5739C= XP_011524025.1:p.Ser1913=
XM_011525724.1:c.5682C= XP_011524026.1:p.Ser1894=
XM_011525725.1:c.5649C= XP_011524027.1:p.Ser1883=
XM_011525726.1:c.5739C= XP_011524028.1:p.Ser1913=
XM_011525723.3:c.5739C= XP_011524025.1:p.Ser1913=
XM_011525724.3:c.5682C= XP_011524026.1:p.Ser1894=
XM_011525725.3:c.5649C= XP_011524027.1:p.Ser1883=
XM_011525726.3:c.5739C= XP_011524028.1:p.Ser1913=
XM_017025918.2:c.5700C= XP_016881407.1:p.Ser1900=
XR_001753259.2:n.6736C=
NM_001378183.1:c.5946C= MANE Select NP_001365112.1:p.Ser1982=
NM_022068.4:c.5607C= NP_071351.2:p.Ser1869=