Canonical Allele Identifier: CA502866525

Gene: PIEZO2

Linked Data

• gnomAD v4: 18-10705218-C-T
• MyVariant Identifiers: chr18:g.10705216C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10705218C>T , CM000680.2:g.10705218C>T	GRCh38
NC_000018.9:g.10705216C>T , CM000680.1:g.10705216C>T	GRCh37
NC_000018.8:g.10695216C>T	NCBI36
NG_034005.1:g.448545G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.5735+118G>A	ENSP00000372900.4:n.5735+118G>A
ENST00000674853.1:c.5999+118G>A MANE Select	ENSP00000501957.1:n.5999+118G>A
ENST00000302079.10:c.5660+118G>A	ENSP00000303316.6:n.5660+118G>A
ENST00000383408.6:c.5513+118G>A	ENSP00000372900.3:n.5513+118G>A
ENST00000503781.7:c.5660+118G>A	ENSP00000421377.3:n.5660+118G>A
ENST00000580640.5:c.5735+118G>A	ENSP00000463094.1:n.5735+118G>A
ENST00000582913.5:c.5866+118G>A	ENSP00000462115.1:n.5866+118G>A
NM_022068.3:c.5660+118G>A	NP_071351.2:n.5660+118G>A
XM_011525723.1:c.5792+118G>A	XP_011524025.1:n.5792+118G>A
XM_011525724.1:c.5735+118G>A	XP_011524026.1:n.5735+118G>A
XM_011525725.1:c.5702+118G>A	XP_011524027.1:n.5702+118G>A
XM_011525726.1:c.5792+118G>A	XP_011524028.1:n.5792+118G>A
XM_011525723.3:c.5792+118G>A	XP_011524025.1:n.5792+118G>A
XM_011525724.3:c.5735+118G>A	XP_011524026.1:n.5735+118G>A
XM_011525725.3:c.5702+118G>A	XP_011524027.1:n.5702+118G>A
XM_011525726.3:c.5792+118G>A	XP_011524028.1:n.5792+118G>A
XM_017025918.2:c.5753+118G>A	XP_016881407.1:n.5753+118G>A
XR_001753259.2:n.6789+118G>A
NM_001378183.1:c.5999+118G>A MANE Select	NP_001365112.1:n.5999+118G>A
NM_022068.4:c.5660+118G>A	NP_071351.2:n.5660+118G>A