Canonical Allele Identifier: CA2284425256

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705412G= , CM000680.2:g.10705412G=	GRCh38
NC_000018.9:g.10705410G= , CM000680.1:g.10705410G=	GRCh37
NC_000018.8:g.10695410G=	NCBI36
NG_034005.1:g.448351C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.5659C=	ENSP00000372900.4:p.Arg1887=
ENST00000643712.1:c.667C=	ENSP00000493635.1:p.Arg223=
ENST00000674853.1:c.5923C= MANE Select	ENSP00000501957.1:p.Arg1975=
ENST00000302079.10:c.5584C=	ENSP00000303316.6:p.Arg1862=
ENST00000383408.6:c.5437C=	ENSP00000372900.3:p.Arg1813=
ENST00000503781.7:c.5584C=	ENSP00000421377.3:p.Arg1862=
ENST00000580640.5:c.5659C=	ENSP00000463094.1:p.Arg1887=
ENST00000582913.5:c.5790C=	ENSP00000462115.1:n.5790C=
NM_022068.3:c.5584C=	NP_071351.2:p.Arg1862=
XM_011525723.1:c.5716C=	XP_011524025.1:p.Arg1906=
XM_011525724.1:c.5659C=	XP_011524026.1:p.Arg1887=
XM_011525725.1:c.5626C=	XP_011524027.1:p.Arg1876=
XM_011525726.1:c.5716C=	XP_011524028.1:p.Arg1906=
XM_011525723.3:c.5716C=	XP_011524025.1:p.Arg1906=
XM_011525724.3:c.5659C=	XP_011524026.1:p.Arg1887=
XM_011525725.3:c.5626C=	XP_011524027.1:p.Arg1876=
XM_011525726.3:c.5716C=	XP_011524028.1:p.Arg1906=
XM_017025918.2:c.5677C=	XP_016881407.1:p.Arg1893=
XR_001753259.2:n.6713C=
NM_001378183.1:c.5923C= MANE Select	NP_001365112.1:p.Arg1975=
NM_022068.4:c.5584C=	NP_071351.2:p.Arg1862=