Canonical Allele Identifier: CA503243207
Gene: PIEZO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.10705396C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705398C>T , CM000680.2:g.10705398C>T GRCh38
NC_000018.9:g.10705396C>T , CM000680.1:g.10705396C>T GRCh37
NC_000018.8:g.10695396C>T NCBI36
NG_034005.1:g.448365G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000383408.7:c.5673G>A ENSP00000372900.4:p.Leu1891=
ENST00000643712.1:c.681G>A ENSP00000493635.1:p.Leu227=
ENST00000674853.1:c.5937G>A MANE Select ENSP00000501957.1:p.Leu1979=
ENST00000302079.10:c.5598G>A ENSP00000303316.6:p.Leu1866=
ENST00000383408.6:c.5451G>A ENSP00000372900.3:p.Leu1817=
ENST00000503781.7:c.5598G>A ENSP00000421377.3:p.Leu1866=
ENST00000580640.5:c.5673G>A ENSP00000463094.1:p.Leu1891=
ENST00000582913.5:c.5804G>A ENSP00000462115.1:n.5804G>A
NM_022068.3:c.5598G>A NP_071351.2:p.Leu1866=
XM_011525723.1:c.5730G>A XP_011524025.1:p.Leu1910=
XM_011525724.1:c.5673G>A XP_011524026.1:p.Leu1891=
XM_011525725.1:c.5640G>A XP_011524027.1:p.Leu1880=
XM_011525726.1:c.5730G>A XP_011524028.1:p.Leu1910=
XM_011525723.3:c.5730G>A XP_011524025.1:p.Leu1910=
XM_011525724.3:c.5673G>A XP_011524026.1:p.Leu1891=
XM_011525725.3:c.5640G>A XP_011524027.1:p.Leu1880=
XM_011525726.3:c.5730G>A XP_011524028.1:p.Leu1910=
XM_017025918.2:c.5691G>A XP_016881407.1:p.Leu1897=
XR_001753259.2:n.6727G>A
NM_001378183.1:c.5937G>A MANE Select NP_001365112.1:p.Leu1979=
NM_022068.4:c.5598G>A NP_071351.2:p.Leu1866=