Canonical Allele Identifier: CA503243202
Gene: PIEZO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.10705390G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705392G>T , CM000680.2:g.10705392G>T GRCh38
NC_000018.9:g.10705390G>T , CM000680.1:g.10705390G>T GRCh37
NC_000018.8:g.10695390G>T NCBI36
NG_034005.1:g.448371C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000383408.7:c.5679C>A ENSP00000372900.4:p.Ser1893=
ENST00000643712.1:c.687C>A ENSP00000493635.1:p.Ser229=
ENST00000674853.1:c.5943C>A MANE Select ENSP00000501957.1:p.Ser1981=
ENST00000302079.10:c.5604C>A ENSP00000303316.6:p.Ser1868=
ENST00000383408.6:c.5457C>A ENSP00000372900.3:p.Ser1819=
ENST00000503781.7:c.5604C>A ENSP00000421377.3:p.Ser1868=
ENST00000580640.5:c.5679C>A ENSP00000463094.1:p.Ser1893=
ENST00000582913.5:c.5810C>A ENSP00000462115.1:n.5810C>A
NM_022068.3:c.5604C>A NP_071351.2:p.Ser1868=
XM_011525723.1:c.5736C>A XP_011524025.1:p.Ser1912=
XM_011525724.1:c.5679C>A XP_011524026.1:p.Ser1893=
XM_011525725.1:c.5646C>A XP_011524027.1:p.Ser1882=
XM_011525726.1:c.5736C>A XP_011524028.1:p.Ser1912=
XM_011525723.3:c.5736C>A XP_011524025.1:p.Ser1912=
XM_011525724.3:c.5679C>A XP_011524026.1:p.Ser1893=
XM_011525725.3:c.5646C>A XP_011524027.1:p.Ser1882=
XM_011525726.3:c.5736C>A XP_011524028.1:p.Ser1912=
XM_017025918.2:c.5697C>A XP_016881407.1:p.Ser1899=
XR_001753259.2:n.6733C>A
NM_001378183.1:c.5943C>A MANE Select NP_001365112.1:p.Ser1981=
NM_022068.4:c.5604C>A NP_071351.2:p.Ser1868=