Canonical Allele Identifier: CA2284452430
Gene: PIEZO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10762556C= , CM000680.2:g.10762556C= GRCh38
NC_000018.9:g.10762554C= , CM000680.1:g.10762554C= GRCh37
NC_000018.8:g.10752554C= NCBI36
NG_034005.1:g.391207G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.3193G= ENSP00000372900.4:p.Asp1065=
ENST00000686869.1:n.3250G=
ENST00000674853.1:c.3193G= MANE Select ENSP00000501957.1:p.Asp1065=
ENST00000302079.10:c.3118G= ENSP00000303316.6:p.Asp1040=
ENST00000383408.6:c.2971G= ENSP00000372900.3:p.Asp991=
ENST00000503781.7:c.3118G= ENSP00000421377.3:p.Asp1040=
ENST00000580640.5:c.3193G= ENSP00000463094.1:p.Asp1065=
ENST00000582913.5:c.3160G= ENSP00000462115.1:p.Asp1054=
NM_022068.3:c.3118G= NP_071351.2:p.Asp1040=
XM_011525723.1:c.3250G= XP_011524025.1:p.Asp1084=
XM_011525724.1:c.3193G= XP_011524026.1:p.Asp1065=
XM_011525725.1:c.3160G= XP_011524027.1:p.Asp1054=
XM_011525726.1:c.3250G= XP_011524028.1:p.Asp1084=
XM_011525727.1:c.3250G= XP_011524029.1:p.Asp1084=
XM_011525723.3:c.3250G= XP_011524025.1:p.Asp1084=
XM_011525724.3:c.3193G= XP_011524026.1:p.Asp1065=
XM_011525725.3:c.3160G= XP_011524027.1:p.Asp1054=
XM_011525726.3:c.3250G= XP_011524028.1:p.Asp1084=
XM_017025918.2:c.3211G= XP_016881407.1:p.Asp1071=
XR_001753259.2:n.4247G=
NM_001378183.1:c.3193G= MANE Select NP_001365112.1:p.Asp1065=
NM_022068.4:c.3118G= NP_071351.2:p.Asp1040=