Canonical Allele Identifier: CA2284425158
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705220C= , CM000680.2:g.10705220C= GRCh38
NC_000018.9:g.10705218C= , CM000680.1:g.10705218C= GRCh37
NC_000018.8:g.10695218C= NCBI36
NG_034005.1:g.448543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5735+116G= ENSP00000372900.4:n.5735+116G=
ENST00000674853.1:c.5999+116G= MANE Select ENSP00000501957.1:n.5999+116G=
ENST00000302079.10:c.5660+116G= ENSP00000303316.6:n.5660+116G=
ENST00000383408.6:c.5513+116G= ENSP00000372900.3:n.5513+116G=
ENST00000503781.7:c.5660+116G= ENSP00000421377.3:n.5660+116G=
ENST00000580640.5:c.5735+116G= ENSP00000463094.1:n.5735+116G=
ENST00000582913.5:c.5866+116G= ENSP00000462115.1:n.5866+116G=
NM_022068.3:c.5660+116G= NP_071351.2:n.5660+116G=
XM_011525723.1:c.5792+116G= XP_011524025.1:n.5792+116G=
XM_011525724.1:c.5735+116G= XP_011524026.1:n.5735+116G=
XM_011525725.1:c.5702+116G= XP_011524027.1:n.5702+116G=
XM_011525726.1:c.5792+116G= XP_011524028.1:n.5792+116G=
XM_011525723.3:c.5792+116G= XP_011524025.1:n.5792+116G=
XM_011525724.3:c.5735+116G= XP_011524026.1:n.5735+116G=
XM_011525725.3:c.5702+116G= XP_011524027.1:n.5702+116G=
XM_011525726.3:c.5792+116G= XP_011524028.1:n.5792+116G=
XM_017025918.2:c.5753+116G= XP_016881407.1:n.5753+116G=
XR_001753259.2:n.6789+116G=
NM_001378183.1:c.5999+116G= MANE Select NP_001365112.1:n.5999+116G=
NM_022068.4:c.5660+116G= NP_071351.2:n.5660+116G=