Canonical Allele Identifier: CA2284425229

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705357G= , CM000680.2:g.10705357G=	GRCh38
NC_000018.9:g.10705355G= , CM000680.1:g.10705355G=	GRCh37
NC_000018.8:g.10695355G=	NCBI36
NG_034005.1:g.448406C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.5714C=	ENSP00000372900.4:p.Ala1905=
ENST00000643712.1:c.722C=	ENSP00000493635.1:p.Ala241=
ENST00000674853.1:c.5978C= MANE Select	ENSP00000501957.1:p.Ala1993=
ENST00000302079.10:c.5639C=	ENSP00000303316.6:p.Ala1880=
ENST00000383408.6:c.5492C=	ENSP00000372900.3:p.Ala1831=
ENST00000503781.7:c.5639C=	ENSP00000421377.3:p.Ala1880=
ENST00000580640.5:c.5714C=	ENSP00000463094.1:p.Ala1905=
ENST00000582913.5:c.5845C=	ENSP00000462115.1:n.5845C=
NM_022068.3:c.5639C=	NP_071351.2:p.Ala1880=
XM_011525723.1:c.5771C=	XP_011524025.1:p.Ala1924=
XM_011525724.1:c.5714C=	XP_011524026.1:p.Ala1905=
XM_011525725.1:c.5681C=	XP_011524027.1:p.Ala1894=
XM_011525726.1:c.5771C=	XP_011524028.1:p.Ala1924=
XM_011525723.3:c.5771C=	XP_011524025.1:p.Ala1924=
XM_011525724.3:c.5714C=	XP_011524026.1:p.Ala1905=
XM_011525725.3:c.5681C=	XP_011524027.1:p.Ala1894=
XM_011525726.3:c.5771C=	XP_011524028.1:p.Ala1924=
XM_017025918.2:c.5732C=	XP_016881407.1:p.Ala1911=
XR_001753259.2:n.6768C=
NM_001378183.1:c.5978C= MANE Select	NP_001365112.1:p.Ala1993=
NM_022068.4:c.5639C=	NP_071351.2:p.Ala1880=