Canonical Allele Identifier: CA401910324
Gene: PIEZO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705393G>T , CM000680.2:g.10705393G>T GRCh38
NC_000018.9:g.10705391G>T , CM000680.1:g.10705391G>T GRCh37
NC_000018.8:g.10695391G>T NCBI36
NG_034005.1:g.448370C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5678C>A ENSP00000372900.4:p.Ser1893Tyr
ENST00000643712.1:c.686C>A ENSP00000493635.1:p.Ser229Tyr
ENST00000674853.1:c.5942C>A MANE Select ENSP00000501957.1:p.Ser1981Tyr
ENST00000302079.10:c.5603C>A ENSP00000303316.6:p.Ser1868Tyr
ENST00000383408.6:c.5456C>A ENSP00000372900.3:p.Ser1819Tyr
ENST00000503781.7:c.5603C>A ENSP00000421377.3:p.Ser1868Tyr
ENST00000580640.5:c.5678C>A ENSP00000463094.1:p.Ser1893Tyr
ENST00000582913.5:c.5809C>A ENSP00000462115.1:n.5809C>A
NM_022068.3:c.5603C>A NP_071351.2:p.Ser1868Tyr
XM_011525723.1:c.5735C>A XP_011524025.1:p.Ser1912Tyr
XM_011525724.1:c.5678C>A XP_011524026.1:p.Ser1893Tyr
XM_011525725.1:c.5645C>A XP_011524027.1:p.Ser1882Tyr
XM_011525726.1:c.5735C>A XP_011524028.1:p.Ser1912Tyr
XM_011525723.3:c.5735C>A XP_011524025.1:p.Ser1912Tyr
XM_011525724.3:c.5678C>A XP_011524026.1:p.Ser1893Tyr
XM_011525725.3:c.5645C>A XP_011524027.1:p.Ser1882Tyr
XM_011525726.3:c.5735C>A XP_011524028.1:p.Ser1912Tyr
XM_017025918.2:c.5696C>A XP_016881407.1:p.Ser1899Tyr
XR_001753259.2:n.6732C>A
NM_001378183.1:c.5942C>A MANE Select NP_001365112.1:p.Ser1981Tyr
NM_022068.4:c.5603C>A NP_071351.2:p.Ser1868Tyr