Canonical Allele Identifier: CA401910328
Gene: PIEZO2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705394A>G , CM000680.2:g.10705394A>G GRCh38
NC_000018.9:g.10705392A>G , CM000680.1:g.10705392A>G GRCh37
NC_000018.8:g.10695392A>G NCBI36
NG_034005.1:g.448369T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5677T>C ENSP00000372900.4:p.Ser1893Pro
ENST00000643712.1:c.685T>C ENSP00000493635.1:p.Ser229Pro
ENST00000674853.1:c.5941T>C MANE Select ENSP00000501957.1:p.Ser1981Pro
ENST00000302079.10:c.5602T>C ENSP00000303316.6:p.Ser1868Pro
ENST00000383408.6:c.5455T>C ENSP00000372900.3:p.Ser1819Pro
ENST00000503781.7:c.5602T>C ENSP00000421377.3:p.Ser1868Pro
ENST00000580640.5:c.5677T>C ENSP00000463094.1:p.Ser1893Pro
ENST00000582913.5:c.5808T>C ENSP00000462115.1:n.5808T>C
NM_022068.3:c.5602T>C NP_071351.2:p.Ser1868Pro
XM_011525723.1:c.5734T>C XP_011524025.1:p.Ser1912Pro
XM_011525724.1:c.5677T>C XP_011524026.1:p.Ser1893Pro
XM_011525725.1:c.5644T>C XP_011524027.1:p.Ser1882Pro
XM_011525726.1:c.5734T>C XP_011524028.1:p.Ser1912Pro
XM_011525723.3:c.5734T>C XP_011524025.1:p.Ser1912Pro
XM_011525724.3:c.5677T>C XP_011524026.1:p.Ser1893Pro
XM_011525725.3:c.5644T>C XP_011524027.1:p.Ser1882Pro
XM_011525726.3:c.5734T>C XP_011524028.1:p.Ser1912Pro
XM_017025918.2:c.5695T>C XP_016881407.1:p.Ser1899Pro
XR_001753259.2:n.6731T>C
NM_001378183.1:c.5941T>C MANE Select NP_001365112.1:p.Ser1981Pro
NM_022068.4:c.5602T>C NP_071351.2:p.Ser1868Pro