Canonical Allele Identifier: CA2284425161
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705229C= , CM000680.2:g.10705229C= GRCh38
NC_000018.9:g.10705227C= , CM000680.1:g.10705227C= GRCh37
NC_000018.8:g.10695227C= NCBI36
NG_034005.1:g.448534G=

Transcript Alleles

HGVS Amino-acid change
ENST00000383408.7:c.5735+107G= ENSP00000372900.4:n.5735+107G=
ENST00000674853.1:c.5999+107G= MANE Select ENSP00000501957.1:n.5999+107G=
ENST00000302079.10:c.5660+107G= ENSP00000303316.6:n.5660+107G=
ENST00000383408.6:c.5513+107G= ENSP00000372900.3:n.5513+107G=
ENST00000503781.7:c.5660+107G= ENSP00000421377.3:n.5660+107G=
ENST00000580640.5:c.5735+107G= ENSP00000463094.1:n.5735+107G=
ENST00000582913.5:c.5866+107G= ENSP00000462115.1:n.5866+107G=
NM_022068.3:c.5660+107G= NP_071351.2:n.5660+107G=
XM_011525723.1:c.5792+107G= XP_011524025.1:n.5792+107G=
XM_011525724.1:c.5735+107G= XP_011524026.1:n.5735+107G=
XM_011525725.1:c.5702+107G= XP_011524027.1:n.5702+107G=
XM_011525726.1:c.5792+107G= XP_011524028.1:n.5792+107G=
XM_011525723.3:c.5792+107G= XP_011524025.1:n.5792+107G=
XM_011525724.3:c.5735+107G= XP_011524026.1:n.5735+107G=
XM_011525725.3:c.5702+107G= XP_011524027.1:n.5702+107G=
XM_011525726.3:c.5792+107G= XP_011524028.1:n.5792+107G=
XM_017025918.2:c.5753+107G= XP_016881407.1:n.5753+107G=
XR_001753259.2:n.6789+107G=
NM_001378183.1:c.5999+107G= MANE Select NP_001365112.1:n.5999+107G=
NM_022068.4:c.5660+107G= NP_071351.2:n.5660+107G=