Canonical Allele Identifier: CA2284467626
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10794885C= , CM000680.2:g.10794885C= GRCh38
NC_000018.9:g.10794883C= , CM000680.1:g.10794883C= GRCh37
NC_000018.8:g.10784883C= NCBI36
NG_034005.1:g.358878G=

Transcript Alleles

HGVS Amino-acid change
ENST00000383408.7:c.1645G= ENSP00000372900.4:p.Val549=
ENST00000686869.1:n.1702G=
ENST00000674853.1:c.1645G= MANE Select ENSP00000501957.1:p.Val549=
ENST00000302079.10:c.1645G= ENSP00000303316.6:p.Val549=
ENST00000383408.6:c.1492G= ENSP00000372900.3:p.Val498=
ENST00000503781.7:c.1645G= ENSP00000421377.3:p.Val549=
ENST00000580640.5:c.1645G= ENSP00000463094.1:p.Val549=
ENST00000582913.5:c.1645G= ENSP00000462115.1:p.Val549=
NM_022068.3:c.1645G= NP_071351.2:p.Val549=
XM_011525723.1:c.1645G= XP_011524025.1:p.Val549=
XM_011525724.1:c.1645G= XP_011524026.1:p.Val549=
XM_011525725.1:c.1645G= XP_011524027.1:p.Val549=
XM_011525726.1:c.1645G= XP_011524028.1:p.Val549=
XM_011525727.1:c.1645G= XP_011524029.1:p.Val549=
XM_011525723.3:c.1645G= XP_011524025.1:p.Val549=
XM_011525724.3:c.1645G= XP_011524026.1:p.Val549=
XM_011525725.3:c.1645G= XP_011524027.1:p.Val549=
XM_011525726.3:c.1645G= XP_011524028.1:p.Val549=
XM_017025918.2:c.1606G= XP_016881407.1:p.Val536=
XR_001753259.2:n.2642G=
NM_001378183.1:c.1645G= MANE Select NP_001365112.1:p.Val549=
NM_022068.4:c.1645G= NP_071351.2:p.Val549=