Canonical Allele Identifier: CA2284425259

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705418C= , CM000680.2:g.10705418C=	GRCh38
NC_000018.9:g.10705416C= , CM000680.1:g.10705416C=	GRCh37
NC_000018.8:g.10695416C=	NCBI36
NG_034005.1:g.448345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.5653G=	ENSP00000372900.4:p.Asp1885=
ENST00000643712.1:c.661G=	ENSP00000493635.1:p.Asp221=
ENST00000674853.1:c.5917G= MANE Select	ENSP00000501957.1:p.Asp1973=
ENST00000302079.10:c.5578G=	ENSP00000303316.6:p.Asp1860=
ENST00000383408.6:c.5431G=	ENSP00000372900.3:p.Asp1811=
ENST00000503781.7:c.5578G=	ENSP00000421377.3:p.Asp1860=
ENST00000580640.5:c.5653G=	ENSP00000463094.1:p.Asp1885=
ENST00000582913.5:c.5784G=	ENSP00000462115.1:n.5784G=
NM_022068.3:c.5578G=	NP_071351.2:p.Asp1860=
XM_011525723.1:c.5710G=	XP_011524025.1:p.Asp1904=
XM_011525724.1:c.5653G=	XP_011524026.1:p.Asp1885=
XM_011525725.1:c.5620G=	XP_011524027.1:p.Asp1874=
XM_011525726.1:c.5710G=	XP_011524028.1:p.Asp1904=
XM_011525723.3:c.5710G=	XP_011524025.1:p.Asp1904=
XM_011525724.3:c.5653G=	XP_011524026.1:p.Asp1885=
XM_011525725.3:c.5620G=	XP_011524027.1:p.Asp1874=
XM_011525726.3:c.5710G=	XP_011524028.1:p.Asp1904=
XM_017025918.2:c.5671G=	XP_016881407.1:p.Asp1891=
XR_001753259.2:n.6707G=
NM_001378183.1:c.5917G= MANE Select	NP_001365112.1:p.Asp1973=
NM_022068.4:c.5578G=	NP_071351.2:p.Asp1860=