Canonical Allele Identifier: CA503243131
Gene: PIEZO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.10705336T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705338T>C , CM000680.2:g.10705338T>C GRCh38
NC_000018.9:g.10705336T>C , CM000680.1:g.10705336T>C GRCh37
NC_000018.8:g.10695336T>C NCBI36
NG_034005.1:g.448425A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5733A>G ENSP00000372900.4:p.Lys1911=
ENST00000643712.1:c.741A>G ENSP00000493635.1:p.Lys247=
ENST00000674853.1:c.5997A>G MANE Select ENSP00000501957.1:p.Lys1999=
ENST00000302079.10:c.5658A>G ENSP00000303316.6:p.Lys1886=
ENST00000383408.6:c.5511A>G ENSP00000372900.3:p.Lys1837=
ENST00000503781.7:c.5658A>G ENSP00000421377.3:p.Lys1886=
ENST00000580640.5:c.5733A>G ENSP00000463094.1:p.Lys1911=
ENST00000582913.5:c.5864A>G ENSP00000462115.1:n.5864A>G
NM_022068.3:c.5658A>G NP_071351.2:p.Lys1886=
XM_011525723.1:c.5790A>G XP_011524025.1:p.Lys1930=
XM_011525724.1:c.5733A>G XP_011524026.1:p.Lys1911=
XM_011525725.1:c.5700A>G XP_011524027.1:p.Lys1900=
XM_011525726.1:c.5790A>G XP_011524028.1:p.Lys1930=
XM_011525723.3:c.5790A>G XP_011524025.1:p.Lys1930=
XM_011525724.3:c.5733A>G XP_011524026.1:p.Lys1911=
XM_011525725.3:c.5700A>G XP_011524027.1:p.Lys1900=
XM_011525726.3:c.5790A>G XP_011524028.1:p.Lys1930=
XM_017025918.2:c.5751A>G XP_016881407.1:p.Lys1917=
XR_001753259.2:n.6787A>G
NM_001378183.1:c.5997A>G MANE Select NP_001365112.1:p.Lys1999=
NM_022068.4:c.5658A>G NP_071351.2:p.Lys1886=