Canonical Allele Identifier: CA503243134

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10705339C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705341C>T , CM000680.2:g.10705341C>T	GRCh38
NC_000018.9:g.10705339C>T , CM000680.1:g.10705339C>T	GRCh37
NC_000018.8:g.10695339C>T	NCBI36
NG_034005.1:g.448422G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.5730G>A	ENSP00000372900.4:p.Leu1910=
ENST00000643712.1:c.738G>A	ENSP00000493635.1:p.Leu246=
ENST00000674853.1:c.5994G>A MANE Select	ENSP00000501957.1:p.Leu1998=
ENST00000302079.10:c.5655G>A	ENSP00000303316.6:p.Leu1885=
ENST00000383408.6:c.5508G>A	ENSP00000372900.3:p.Leu1836=
ENST00000503781.7:c.5655G>A	ENSP00000421377.3:p.Leu1885=
ENST00000580640.5:c.5730G>A	ENSP00000463094.1:p.Leu1910=
ENST00000582913.5:c.5861G>A	ENSP00000462115.1:n.5861G>A
NM_022068.3:c.5655G>A	NP_071351.2:p.Leu1885=
XM_011525723.1:c.5787G>A	XP_011524025.1:p.Leu1929=
XM_011525724.1:c.5730G>A	XP_011524026.1:p.Leu1910=
XM_011525725.1:c.5697G>A	XP_011524027.1:p.Leu1899=
XM_011525726.1:c.5787G>A	XP_011524028.1:p.Leu1929=
XM_011525723.3:c.5787G>A	XP_011524025.1:p.Leu1929=
XM_011525724.3:c.5730G>A	XP_011524026.1:p.Leu1910=
XM_011525725.3:c.5697G>A	XP_011524027.1:p.Leu1899=
XM_011525726.3:c.5787G>A	XP_011524028.1:p.Leu1929=
XM_017025918.2:c.5748G>A	XP_016881407.1:p.Leu1916=
XR_001753259.2:n.6784G>A
NM_001378183.1:c.5994G>A MANE Select	NP_001365112.1:p.Leu1998=
NM_022068.4:c.5655G>A	NP_071351.2:p.Leu1885=