Canonical Allele Identifier: CA401910334

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10705395C>T (hg19) ; chr18:g.10705397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705397C>T , CM000680.2:g.10705397C>T	GRCh38
NC_000018.9:g.10705395C>T , CM000680.1:g.10705395C>T	GRCh37
NC_000018.8:g.10695395C>T	NCBI36
NG_034005.1:g.448366G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.5674G>A	ENSP00000372900.4:p.Gly1892Arg
ENST00000643712.1:c.682G>A	ENSP00000493635.1:p.Gly228Arg
ENST00000674853.1:c.5938G>A MANE Select	ENSP00000501957.1:p.Gly1980Arg
ENST00000302079.10:c.5599G>A	ENSP00000303316.6:p.Gly1867Arg
ENST00000383408.6:c.5452G>A	ENSP00000372900.3:p.Gly1818Arg
ENST00000503781.7:c.5599G>A	ENSP00000421377.3:p.Gly1867Arg
ENST00000580640.5:c.5674G>A	ENSP00000463094.1:p.Gly1892Arg
ENST00000582913.5:c.5805G>A	ENSP00000462115.1:n.5805G>A
NM_022068.3:c.5599G>A	NP_071351.2:p.Gly1867Arg
XM_011525723.1:c.5731G>A	XP_011524025.1:p.Gly1911Arg
XM_011525724.1:c.5674G>A	XP_011524026.1:p.Gly1892Arg
XM_011525725.1:c.5641G>A	XP_011524027.1:p.Gly1881Arg
XM_011525726.1:c.5731G>A	XP_011524028.1:p.Gly1911Arg
XM_011525723.3:c.5731G>A	XP_011524025.1:p.Gly1911Arg
XM_011525724.3:c.5674G>A	XP_011524026.1:p.Gly1892Arg
XM_011525725.3:c.5641G>A	XP_011524027.1:p.Gly1881Arg
XM_011525726.3:c.5731G>A	XP_011524028.1:p.Gly1911Arg
XM_017025918.2:c.5692G>A	XP_016881407.1:p.Gly1898Arg
XR_001753259.2:n.6728G>A
NM_001378183.1:c.5938G>A MANE Select	NP_001365112.1:p.Gly1980Arg
NM_022068.4:c.5599G>A	NP_071351.2:p.Gly1867Arg