Canonical Allele Identifier: CA2284425243

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705382G= , CM000680.2:g.10705382G=	GRCh38
NC_000018.9:g.10705380G= , CM000680.1:g.10705380G=	GRCh37
NC_000018.8:g.10695380G=	NCBI36
NG_034005.1:g.448381C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.5689C=	ENSP00000372900.4:p.Pro1897=
ENST00000643712.1:c.697C=	ENSP00000493635.1:p.Pro233=
ENST00000674853.1:c.5953C= MANE Select	ENSP00000501957.1:p.Pro1985=
ENST00000302079.10:c.5614C=	ENSP00000303316.6:p.Pro1872=
ENST00000383408.6:c.5467C=	ENSP00000372900.3:p.Pro1823=
ENST00000503781.7:c.5614C=	ENSP00000421377.3:p.Pro1872=
ENST00000580640.5:c.5689C=	ENSP00000463094.1:p.Pro1897=
ENST00000582913.5:c.5820C=	ENSP00000462115.1:n.5820C=
NM_022068.3:c.5614C=	NP_071351.2:p.Pro1872=
XM_011525723.1:c.5746C=	XP_011524025.1:p.Pro1916=
XM_011525724.1:c.5689C=	XP_011524026.1:p.Pro1897=
XM_011525725.1:c.5656C=	XP_011524027.1:p.Pro1886=
XM_011525726.1:c.5746C=	XP_011524028.1:p.Pro1916=
XM_011525723.3:c.5746C=	XP_011524025.1:p.Pro1916=
XM_011525724.3:c.5689C=	XP_011524026.1:p.Pro1897=
XM_011525725.3:c.5656C=	XP_011524027.1:p.Pro1886=
XM_011525726.3:c.5746C=	XP_011524028.1:p.Pro1916=
XM_017025918.2:c.5707C=	XP_016881407.1:p.Pro1903=
XR_001753259.2:n.6743C=
NM_001378183.1:c.5953C= MANE Select	NP_001365112.1:p.Pro1985=
NM_022068.4:c.5614C=	NP_071351.2:p.Pro1872=