Canonical Allele Identifier: CA502900389

Gene: PIEZO2

Linked Data

• gnomAD v4: 18-10762539-G-T
• MyVariant Identifiers: chr18:g.10762537G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762539G>T , CM000680.2:g.10762539G>T	GRCh38
NC_000018.9:g.10762537G>T , CM000680.1:g.10762537G>T	GRCh37
NC_000018.8:g.10752537G>T	NCBI36
NG_034005.1:g.391224C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3210C>A	ENSP00000372900.4:p.Val1070=
ENST00000686869.1:n.3267C>A
ENST00000674853.1:c.3210C>A MANE Select	ENSP00000501957.1:p.Val1070=
ENST00000302079.10:c.3135C>A	ENSP00000303316.6:p.Val1045=
ENST00000383408.6:c.2988C>A	ENSP00000372900.3:p.Val996=
ENST00000503781.7:c.3135C>A	ENSP00000421377.3:p.Val1045=
ENST00000580640.5:c.3210C>A	ENSP00000463094.1:p.Val1070=
ENST00000582913.5:c.3177C>A	ENSP00000462115.1:p.Val1059=
NM_022068.3:c.3135C>A	NP_071351.2:p.Val1045=
XM_011525723.1:c.3267C>A	XP_011524025.1:p.Val1089=
XM_011525724.1:c.3210C>A	XP_011524026.1:p.Val1070=
XM_011525725.1:c.3177C>A	XP_011524027.1:p.Val1059=
XM_011525726.1:c.3267C>A	XP_011524028.1:p.Val1089=
XM_011525727.1:c.3267C>A	XP_011524029.1:p.Val1089=
XM_011525723.3:c.3267C>A	XP_011524025.1:p.Val1089=
XM_011525724.3:c.3210C>A	XP_011524026.1:p.Val1070=
XM_011525725.3:c.3177C>A	XP_011524027.1:p.Val1059=
XM_011525726.3:c.3267C>A	XP_011524028.1:p.Val1089=
XM_017025918.2:c.3228C>A	XP_016881407.1:p.Val1076=
XR_001753259.2:n.4264C>A
NM_001378183.1:c.3210C>A MANE Select	NP_001365112.1:p.Val1070=
NM_022068.4:c.3135C>A	NP_071351.2:p.Val1045=