Canonical Allele Identifier: CA2284422296
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10699005del , CM000680.2:g.10699005del GRCh38
NC_000018.9:g.10699003del , CM000680.1:g.10699003del GRCh37
NC_000018.8:g.10689003del NCBI36
NG_034005.1:g.454758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.6350del ENSP00000372900.4:p.Thr2117LysfsTer?
ENST00000685517.1:n.1353del
ENST00000674853.1:c.6614del MANE Select ENSP00000501957.1:p.Thr2205LysfsTer?
ENST00000302079.10:c.6275del ENSP00000303316.6:p.Thr2092LysfsTer?
ENST00000383408.6:c.6128del ENSP00000372900.3:p.Thr2043LysfsTer?
ENST00000503781.7:c.6275del ENSP00000421377.3:p.Thr2092LysfsTer?
ENST00000538948.5:c.146del ENSP00000443129.1:p.Thr49LysfsTer?
ENST00000580640.5:c.6350del ENSP00000463094.1:p.Thr2117LysfsTer?
ENST00000582913.5:c.6481del ENSP00000462115.1:n.6481del
NM_022068.3:c.6275del NP_071351.2:p.Thr2092LysfsTer?
XM_011525723.1:c.6407del XP_011524025.1:p.Thr2136LysfsTer?
XM_011525724.1:c.6350del XP_011524026.1:p.Thr2117LysfsTer?
XM_011525725.1:c.6317del XP_011524027.1:p.Thr2106LysfsTer?
XM_011525726.1:c.6224del XP_011524028.1:p.Thr2075LysfsTer?
XM_011525723.3:c.6407del XP_011524025.1:p.Thr2136LysfsTer?
XM_011525724.3:c.6350del XP_011524026.1:p.Thr2117LysfsTer?
XM_011525725.3:c.6317del XP_011524027.1:p.Thr2106LysfsTer?
XM_011525726.3:c.6224del XP_011524028.1:p.Thr2075LysfsTer?
XM_017025918.2:c.6368del XP_016881407.1:p.Thr2123LysfsTer?
XR_001753259.2:n.7404del
NM_001378183.1:c.6614del MANE Select NP_001365112.1:p.Thr2205LysfsTer?
NM_022068.4:c.6275del NP_071351.2:p.Thr2092LysfsTer?