Canonical Allele Identifier: CA2284409206

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10671729C= , CM000680.2:g.10671729C=	GRCh38
NC_000018.9:g.10671726C= , CM000680.1:g.10671726C=	GRCh37
NC_000018.8:g.10661726C=	NCBI36
NG_034005.1:g.482034G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001378183.1:c.8396G= MANE Select	NP_001365112.1:p.Arg2799=
ENST00000674853.1:c.8396G= MANE Select	ENSP00000501957.1:p.Arg2799=
NM_022068.3:c.8057G=	NP_071351.2:p.Arg2686=
NM_022068.4:c.8057G=	NP_071351.2:p.Arg2686=
ENST00000302079.10:c.7868G=	ENSP00000303316.6:p.Arg2623=
ENST00000383408.6:c.7910G=	ENSP00000372900.3:p.Arg2637=
ENST00000383408.7:c.*1498G=	ENSP00000372900.4:n.*1498G=
ENST00000503781.7:c.8057G=	ENSP00000421377.3:p.Arg2686=
ENST00000538948.5:c.1928G=	ENSP00000443129.1:p.Arg643=
ENST00000580640.5:c.8132G=	ENSP00000463094.1:p.Arg2711=
ENST00000581680.1:n.533G=
ENST00000582913.5:c.8263G=	ENSP00000462115.1:n.8263G=
ENST00000582937.1:c.58+961G=	ENSP00000462187.1:n.58+961G=
ENST00000685517.1:n.3139G=
ENST00000691469.1:n.2294G=
ENST00000693743.1:c.1592G=	ENSP00000510331.1:n.1592G=
XM_011525723.1:c.8189G=	XP_011524025.1:p.Arg2730=
XM_011525723.3:c.8189G=	XP_011524025.1:p.Arg2730=
XM_011525724.1:c.8132G=	XP_011524026.1:p.Arg2711=
XM_011525724.3:c.8132G=	XP_011524026.1:p.Arg2711=
XM_011525725.1:c.8099G=	XP_011524027.1:p.Arg2700=
XM_011525725.3:c.8099G=	XP_011524027.1:p.Arg2700=
XM_011525726.1:c.8006G=	XP_011524028.1:p.Arg2669=
XM_011525726.3:c.8006G=	XP_011524028.1:p.Arg2669=
XM_017025918.2:c.8150G=	XP_016881407.1:p.Arg2717=