Canonical Allele Identifier: CA401913602

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10675261A>T , CM000680.2:g.10675261A>T	GRCh38
NC_000018.9:g.10675258A>T , CM000680.1:g.10675258A>T	GRCh37
NC_000018.8:g.10665258A>T	NCBI36
NG_034005.1:g.478502T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.*1211T>A	ENSP00000372900.4:n.*1211T>A
ENST00000685517.1:n.2852T>A
ENST00000691469.1:n.2007T>A
ENST00000693743.1:c.1305T>A	ENSP00000510331.1:n.1305T>A
ENST00000674853.1:c.8109T>A MANE Select	ENSP00000501957.1:p.Tyr2703Ter
ENST00000302079.10:c.7581T>A	ENSP00000303316.6:p.Tyr2527Ter
ENST00000383408.6:c.7623T>A	ENSP00000372900.3:p.Tyr2541Ter
ENST00000503781.7:c.7770T>A	ENSP00000421377.3:p.Tyr2590Ter
ENST00000538948.5:c.1641T>A	ENSP00000443129.1:p.Tyr547Ter
ENST00000580640.5:c.7845T>A	ENSP00000463094.1:p.Tyr2615Ter
ENST00000581680.1:n.246T>A
ENST00000582913.5:c.7976T>A	ENSP00000462115.1:n.7976T>A
NM_022068.3:c.7770T>A	NP_071351.2:p.Tyr2590Ter
XM_011525723.1:c.7902T>A	XP_011524025.1:p.Tyr2634Ter
XM_011525724.1:c.7845T>A	XP_011524026.1:p.Tyr2615Ter
XM_011525725.1:c.7812T>A	XP_011524027.1:p.Tyr2604Ter
XM_011525726.1:c.7719T>A	XP_011524028.1:p.Tyr2573Ter
XM_011525723.3:c.7902T>A	XP_011524025.1:p.Tyr2634Ter
XM_011525724.3:c.7845T>A	XP_011524026.1:p.Tyr2615Ter
XM_011525725.3:c.7812T>A	XP_011524027.1:p.Tyr2604Ter
XM_011525726.3:c.7719T>A	XP_011524028.1:p.Tyr2573Ter
XM_017025918.2:c.7863T>A	XP_016881407.1:p.Tyr2621Ter
XR_001753259.2:n.8823T>A
NM_001378183.1:c.8109T>A MANE Select	NP_001365112.1:p.Tyr2703Ter
NM_022068.4:c.7770T>A	NP_071351.2:p.Tyr2590Ter