Canonical Allele Identifier: CA401910402

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10705427A>G (hg19) ; chr18:g.10705429A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705429A>G , CM000680.2:g.10705429A>G	GRCh38
NC_000018.9:g.10705427A>G , CM000680.1:g.10705427A>G	GRCh37
NC_000018.8:g.10695427A>G	NCBI36
NG_034005.1:g.448334T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.5642T>C	ENSP00000372900.4:p.Val1881Ala
ENST00000643712.1:c.650T>C	ENSP00000493635.1:p.Val217Ala
ENST00000674853.1:c.5906T>C MANE Select	ENSP00000501957.1:p.Val1969Ala
ENST00000302079.10:c.5567T>C	ENSP00000303316.6:p.Val1856Ala
ENST00000383408.6:c.5420T>C	ENSP00000372900.3:p.Val1807Ala
ENST00000503781.7:c.5567T>C	ENSP00000421377.3:p.Val1856Ala
ENST00000580640.5:c.5642T>C	ENSP00000463094.1:p.Val1881Ala
ENST00000582913.5:c.5773T>C	ENSP00000462115.1:n.5773T>C
NM_022068.3:c.5567T>C	NP_071351.2:p.Val1856Ala
XM_011525723.1:c.5699T>C	XP_011524025.1:p.Val1900Ala
XM_011525724.1:c.5642T>C	XP_011524026.1:p.Val1881Ala
XM_011525725.1:c.5609T>C	XP_011524027.1:p.Val1870Ala
XM_011525726.1:c.5699T>C	XP_011524028.1:p.Val1900Ala
XM_011525723.3:c.5699T>C	XP_011524025.1:p.Val1900Ala
XM_011525724.3:c.5642T>C	XP_011524026.1:p.Val1881Ala
XM_011525725.3:c.5609T>C	XP_011524027.1:p.Val1870Ala
XM_011525726.3:c.5699T>C	XP_011524028.1:p.Val1900Ala
XM_017025918.2:c.5660T>C	XP_016881407.1:p.Val1887Ala
XR_001753259.2:n.6696T>C
NM_001378183.1:c.5906T>C MANE Select	NP_001365112.1:p.Val1969Ala
NM_022068.4:c.5567T>C	NP_071351.2:p.Val1856Ala