Canonical Allele Identifier: CA502893476
Gene: PIEZO2 HGNC NCBI

Linked Data

dbSNP Id: rs1269140926

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10784882C>T , CM000680.2:g.10784882C>T GRCh38
NC_000018.9:g.10784880C>T , CM000680.1:g.10784880C>T GRCh37
NC_000018.8:g.10774880C>T NCBI36
NG_034005.1:g.368881G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.2394G>A ENSP00000372900.4:p.Leu798=
ENST00000686869.1:n.2451G>A
ENST00000674853.1:c.2394G>A MANE Select ENSP00000501957.1:p.Leu798=
ENST00000302079.10:c.2394G>A ENSP00000303316.6:p.Leu798=
ENST00000383408.6:c.2241G>A ENSP00000372900.3:p.Leu747=
ENST00000503781.7:c.2394G>A ENSP00000421377.3:p.Leu798=
ENST00000580640.5:c.2394G>A ENSP00000463094.1:p.Leu798=
ENST00000582913.5:c.2394G>A ENSP00000462115.1:p.Leu798=
ENST00000583325.1:c.381G>A ENSP00000462560.1:p.Leu127=
NM_022068.3:c.2394G>A NP_071351.2:p.Leu798=
XM_011525723.1:c.2394G>A XP_011524025.1:p.Leu798=
XM_011525724.1:c.2394G>A XP_011524026.1:p.Leu798=
XM_011525725.1:c.2394G>A XP_011524027.1:p.Leu798=
XM_011525726.1:c.2394G>A XP_011524028.1:p.Leu798=
XM_011525727.1:c.2394G>A XP_011524029.1:p.Leu798=
XM_011525723.3:c.2394G>A XP_011524025.1:p.Leu798=
XM_011525724.3:c.2394G>A XP_011524026.1:p.Leu798=
XM_011525725.3:c.2394G>A XP_011524027.1:p.Leu798=
XM_011525726.3:c.2394G>A XP_011524028.1:p.Leu798=
XM_017025918.2:c.2355G>A XP_016881407.1:p.Leu785=
XR_001753259.2:n.3391G>A
NM_001378183.1:c.2394G>A MANE Select NP_001365112.1:p.Leu798=
NM_022068.4:c.2394G>A NP_071351.2:p.Leu798=