Canonical Allele Identifier: CA2284409213

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10671730G= , CM000680.2:g.10671730G=	GRCh38
NC_000018.9:g.10671727G= , CM000680.1:g.10671727G=	GRCh37
NC_000018.8:g.10661727G=	NCBI36
NG_034005.1:g.482033C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001378183.1:c.8395C= MANE Select	NP_001365112.1:p.Arg2799=
ENST00000674853.1:c.8395C= MANE Select	ENSP00000501957.1:p.Arg2799=
NM_022068.3:c.8056C=	NP_071351.2:p.Arg2686=
NM_022068.4:c.8056C=	NP_071351.2:p.Arg2686=
ENST00000302079.10:c.7867C=	ENSP00000303316.6:p.Arg2623=
ENST00000383408.6:c.7909C=	ENSP00000372900.3:p.Arg2637=
ENST00000383408.7:c.*1497C=	ENSP00000372900.4:n.*1497C=
ENST00000503781.7:c.8056C=	ENSP00000421377.3:p.Arg2686=
ENST00000538948.5:c.1927C=	ENSP00000443129.1:p.Arg643=
ENST00000580640.5:c.8131C=	ENSP00000463094.1:p.Arg2711=
ENST00000581680.1:n.532C=
ENST00000582913.5:c.8262C=	ENSP00000462115.1:n.8262C=
ENST00000582937.1:c.58+960C=	ENSP00000462187.1:n.58+960C=
ENST00000685517.1:n.3138C=
ENST00000691469.1:n.2293C=
ENST00000693743.1:c.1591C=	ENSP00000510331.1:n.1591C=
XM_011525723.1:c.8188C=	XP_011524025.1:p.Arg2730=
XM_011525723.3:c.8188C=	XP_011524025.1:p.Arg2730=
XM_011525724.1:c.8131C=	XP_011524026.1:p.Arg2711=
XM_011525724.3:c.8131C=	XP_011524026.1:p.Arg2711=
XM_011525725.1:c.8098C=	XP_011524027.1:p.Arg2700=
XM_011525725.3:c.8098C=	XP_011524027.1:p.Arg2700=
XM_011525726.1:c.8005C=	XP_011524028.1:p.Arg2669=
XM_011525726.3:c.8005C=	XP_011524028.1:p.Arg2669=
XM_017025918.2:c.8149C=	XP_016881407.1:p.Arg2717=