Canonical Allele Identifier: CA401910310
Gene: PIEZO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705387A>C , CM000680.2:g.10705387A>C GRCh38
NC_000018.9:g.10705385A>C , CM000680.1:g.10705385A>C GRCh37
NC_000018.8:g.10695385A>C NCBI36
NG_034005.1:g.448376T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000383408.7:c.5684T>G ENSP00000372900.4:p.Ile1895Ser
ENST00000643712.1:c.692T>G ENSP00000493635.1:p.Ile231Ser
ENST00000674853.1:c.5948T>G MANE Select ENSP00000501957.1:p.Ile1983Ser
ENST00000302079.10:c.5609T>G ENSP00000303316.6:p.Ile1870Ser
ENST00000383408.6:c.5462T>G ENSP00000372900.3:p.Ile1821Ser
ENST00000503781.7:c.5609T>G ENSP00000421377.3:p.Ile1870Ser
ENST00000580640.5:c.5684T>G ENSP00000463094.1:p.Ile1895Ser
ENST00000582913.5:c.5815T>G ENSP00000462115.1:n.5815T>G
NM_022068.3:c.5609T>G NP_071351.2:p.Ile1870Ser
XM_011525723.1:c.5741T>G XP_011524025.1:p.Ile1914Ser
XM_011525724.1:c.5684T>G XP_011524026.1:p.Ile1895Ser
XM_011525725.1:c.5651T>G XP_011524027.1:p.Ile1884Ser
XM_011525726.1:c.5741T>G XP_011524028.1:p.Ile1914Ser
XM_011525723.3:c.5741T>G XP_011524025.1:p.Ile1914Ser
XM_011525724.3:c.5684T>G XP_011524026.1:p.Ile1895Ser
XM_011525725.3:c.5651T>G XP_011524027.1:p.Ile1884Ser
XM_011525726.3:c.5741T>G XP_011524028.1:p.Ile1914Ser
XM_017025918.2:c.5702T>G XP_016881407.1:p.Ile1901Ser
XR_001753259.2:n.6738T>G
NM_001378183.1:c.5948T>G MANE Select NP_001365112.1:p.Ile1983Ser
NM_022068.4:c.5609T>G NP_071351.2:p.Ile1870Ser