Canonical Allele Identifier: CA2284425236

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705369T= , CM000680.2:g.10705369T=	GRCh38
NC_000018.9:g.10705367T= , CM000680.1:g.10705367T=	GRCh37
NC_000018.8:g.10695367T=	NCBI36
NG_034005.1:g.448394A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.5702A=	ENSP00000372900.4:p.His1901=
ENST00000643712.1:c.710A=	ENSP00000493635.1:p.His237=
ENST00000674853.1:c.5966A= MANE Select	ENSP00000501957.1:p.His1989=
ENST00000302079.10:c.5627A=	ENSP00000303316.6:p.His1876=
ENST00000383408.6:c.5480A=	ENSP00000372900.3:p.His1827=
ENST00000503781.7:c.5627A=	ENSP00000421377.3:p.His1876=
ENST00000580640.5:c.5702A=	ENSP00000463094.1:p.His1901=
ENST00000582913.5:c.5833A=	ENSP00000462115.1:n.5833A=
NM_022068.3:c.5627A=	NP_071351.2:p.His1876=
XM_011525723.1:c.5759A=	XP_011524025.1:p.His1920=
XM_011525724.1:c.5702A=	XP_011524026.1:p.His1901=
XM_011525725.1:c.5669A=	XP_011524027.1:p.His1890=
XM_011525726.1:c.5759A=	XP_011524028.1:p.His1920=
XM_011525723.3:c.5759A=	XP_011524025.1:p.His1920=
XM_011525724.3:c.5702A=	XP_011524026.1:p.His1901=
XM_011525725.3:c.5669A=	XP_011524027.1:p.His1890=
XM_011525726.3:c.5759A=	XP_011524028.1:p.His1920=
XM_017025918.2:c.5720A=	XP_016881407.1:p.His1907=
XR_001753259.2:n.6756A=
NM_001378183.1:c.5966A= MANE Select	NP_001365112.1:p.His1989=
NM_022068.4:c.5627A=	NP_071351.2:p.His1876=