Canonical Allele Identifier: CA2284429998

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10715678C= , CM000680.2:g.10715678C=	GRCh38
NC_000018.9:g.10715676C= , CM000680.1:g.10715676C=	GRCh37
NC_000018.8:g.10705676C=	NCBI36
NG_034005.1:g.438085G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001378183.1:c.5228G= MANE Select	NP_001365112.1:p.Arg1743=
ENST00000674853.1:c.5228G= MANE Select	ENSP00000501957.1:p.Arg1743=
NM_022068.3:c.5054G=	NP_071351.2:p.Arg1685=
NM_022068.4:c.5054G=	NP_071351.2:p.Arg1685=
ENST00000302079.10:c.5054G=	ENSP00000303316.6:p.Arg1685=
ENST00000383408.6:c.4907G=	ENSP00000372900.3:p.Arg1636=
ENST00000383408.7:c.5129G=	ENSP00000372900.4:p.Arg1710=
ENST00000503781.7:c.5054G=	ENSP00000421377.3:p.Arg1685=
ENST00000580640.5:c.5129G=	ENSP00000463094.1:p.Arg1710=
ENST00000582913.5:c.5095G=	ENSP00000462115.1:n.5095G=
ENST00000686869.1:n.5186G=
XM_011525723.1:c.5186G=	XP_011524025.1:p.Arg1729=
XM_011525723.3:c.5186G=	XP_011524025.1:p.Arg1729=
XM_011525724.1:c.5129G=	XP_011524026.1:p.Arg1710=
XM_011525724.3:c.5129G=	XP_011524026.1:p.Arg1710=
XM_011525725.1:c.5096G=	XP_011524027.1:p.Arg1699=
XM_011525725.3:c.5096G=	XP_011524027.1:p.Arg1699=
XM_011525726.1:c.5186G=	XP_011524028.1:p.Arg1729=
XM_011525726.3:c.5186G=	XP_011524028.1:p.Arg1729=
XM_017025918.2:c.5147G=	XP_016881407.1:p.Arg1716=
XR_001753259.2:n.6183G=