Canonical Allele Identifier: CA2284457525
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10773414G= , CM000680.2:g.10773414G= GRCh38
NC_000018.9:g.10773412G= , CM000680.1:g.10773412G= GRCh37
NC_000018.8:g.10763412G= NCBI36
NG_034005.1:g.380349C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.2783C= ENSP00000372900.4:p.Ser928=
ENST00000686869.1:n.2840C=
ENST00000674853.1:c.2783C= MANE Select ENSP00000501957.1:p.Ser928=
ENST00000302079.10:c.2708C= ENSP00000303316.6:p.Ser903=
ENST00000383408.6:c.2555C= ENSP00000372900.3:p.Ser852=
ENST00000503781.7:c.2708C= ENSP00000421377.3:p.Ser903=
ENST00000578145.1:n.151C=
ENST00000580640.5:c.2783C= ENSP00000463094.1:p.Ser928=
ENST00000582913.5:c.2750C= ENSP00000462115.1:p.Ser917=
NM_022068.3:c.2708C= NP_071351.2:p.Ser903=
XM_011525723.1:c.2840C= XP_011524025.1:p.Ser947=
XM_011525724.1:c.2783C= XP_011524026.1:p.Ser928=
XM_011525725.1:c.2750C= XP_011524027.1:p.Ser917=
XM_011525726.1:c.2840C= XP_011524028.1:p.Ser947=
XM_011525727.1:c.2840C= XP_011524029.1:p.Ser947=
XM_011525723.3:c.2840C= XP_011524025.1:p.Ser947=
XM_011525724.3:c.2783C= XP_011524026.1:p.Ser928=
XM_011525725.3:c.2750C= XP_011524027.1:p.Ser917=
XM_011525726.3:c.2840C= XP_011524028.1:p.Ser947=
XM_017025918.2:c.2801C= XP_016881407.1:p.Ser934=
XR_001753259.2:n.3837C=
NM_001378183.1:c.2783C= MANE Select NP_001365112.1:p.Ser928=
NM_022068.4:c.2708C= NP_071351.2:p.Ser903=