Canonical Allele Identifier: CA503243182

Gene: PIEZO2

Linked Data

• gnomAD v4: 18-10705377-G-A
• MyVariant Identifiers: chr18:g.10705375G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705377G>A , CM000680.2:g.10705377G>A	GRCh38
NC_000018.9:g.10705375G>A , CM000680.1:g.10705375G>A	GRCh37
NC_000018.8:g.10695375G>A	NCBI36
NG_034005.1:g.448386C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.5694C>T	ENSP00000372900.4:p.Pro1898=
ENST00000643712.1:c.702C>T	ENSP00000493635.1:p.Pro234=
ENST00000674853.1:c.5958C>T MANE Select	ENSP00000501957.1:p.Pro1986=
ENST00000302079.10:c.5619C>T	ENSP00000303316.6:p.Pro1873=
ENST00000383408.6:c.5472C>T	ENSP00000372900.3:p.Pro1824=
ENST00000503781.7:c.5619C>T	ENSP00000421377.3:p.Pro1873=
ENST00000580640.5:c.5694C>T	ENSP00000463094.1:p.Pro1898=
ENST00000582913.5:c.5825C>T	ENSP00000462115.1:n.5825C>T
NM_022068.3:c.5619C>T	NP_071351.2:p.Pro1873=
XM_011525723.1:c.5751C>T	XP_011524025.1:p.Pro1917=
XM_011525724.1:c.5694C>T	XP_011524026.1:p.Pro1898=
XM_011525725.1:c.5661C>T	XP_011524027.1:p.Pro1887=
XM_011525726.1:c.5751C>T	XP_011524028.1:p.Pro1917=
XM_011525723.3:c.5751C>T	XP_011524025.1:p.Pro1917=
XM_011525724.3:c.5694C>T	XP_011524026.1:p.Pro1898=
XM_011525725.3:c.5661C>T	XP_011524027.1:p.Pro1887=
XM_011525726.3:c.5751C>T	XP_011524028.1:p.Pro1917=
XM_017025918.2:c.5712C>T	XP_016881407.1:p.Pro1904=
XR_001753259.2:n.6748C>T
NM_001378183.1:c.5958C>T MANE Select	NP_001365112.1:p.Pro1986=
NM_022068.4:c.5619C>T	NP_071351.2:p.Pro1873=