Canonical Allele Identifier: CA503243183

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10705378A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705380A>C , CM000680.2:g.10705380A>C	GRCh38
NC_000018.9:g.10705378A>C , CM000680.1:g.10705378A>C	GRCh37
NC_000018.8:g.10695378A>C	NCBI36
NG_034005.1:g.448383T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.5691T>G	ENSP00000372900.4:p.Pro1897=
ENST00000643712.1:c.699T>G	ENSP00000493635.1:p.Pro233=
ENST00000674853.1:c.5955T>G MANE Select	ENSP00000501957.1:p.Pro1985=
ENST00000302079.10:c.5616T>G	ENSP00000303316.6:p.Pro1872=
ENST00000383408.6:c.5469T>G	ENSP00000372900.3:p.Pro1823=
ENST00000503781.7:c.5616T>G	ENSP00000421377.3:p.Pro1872=
ENST00000580640.5:c.5691T>G	ENSP00000463094.1:p.Pro1897=
ENST00000582913.5:c.5822T>G	ENSP00000462115.1:n.5822T>G
NM_022068.3:c.5616T>G	NP_071351.2:p.Pro1872=
XM_011525723.1:c.5748T>G	XP_011524025.1:p.Pro1916=
XM_011525724.1:c.5691T>G	XP_011524026.1:p.Pro1897=
XM_011525725.1:c.5658T>G	XP_011524027.1:p.Pro1886=
XM_011525726.1:c.5748T>G	XP_011524028.1:p.Pro1916=
XM_011525723.3:c.5748T>G	XP_011524025.1:p.Pro1916=
XM_011525724.3:c.5691T>G	XP_011524026.1:p.Pro1897=
XM_011525725.3:c.5658T>G	XP_011524027.1:p.Pro1886=
XM_011525726.3:c.5748T>G	XP_011524028.1:p.Pro1916=
XM_017025918.2:c.5709T>G	XP_016881407.1:p.Pro1903=
XR_001753259.2:n.6745T>G
NM_001378183.1:c.5955T>G MANE Select	NP_001365112.1:p.Pro1985=
NM_022068.4:c.5616T>G	NP_071351.2:p.Pro1872=