Canonical Allele Identifier: CA14529540

Gene: PIEZO2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10923810G>T , CM000680.2:g.10923810G>T	GRCh38
NC_000018.9:g.10923808G>T , CM000680.1:g.10923808G>T	GRCh37
NC_000018.8:g.10913808G>T	NCBI36
NG_034005.1:g.229953C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.287-12582C>A	ENSP00000372900.4:n.287-12582C>A
ENST00000686869.1:n.344-12582C>A
ENST00000674853.1:c.287-12582C>A MANE Select	ENSP00000501957.1:n.287-12582C>A
ENST00000302079.10:c.287-12582C>A	ENSP00000303316.6:n.287-12582C>A
ENST00000383408.6:c.134-12582C>A	ENSP00000372900.3:n.134-12582C>A
ENST00000503781.7:c.287-12582C>A	ENSP00000421377.3:n.287-12582C>A
ENST00000580640.5:c.287-12582C>A	ENSP00000463094.1:n.287-12582C>A
ENST00000582913.5:c.287-12582C>A	ENSP00000462115.1:n.287-12582C>A
NM_022068.3:c.287-12582C>A	NP_071351.2:n.287-12582C>A
XM_011525723.1:c.287-12582C>A	XP_011524025.1:n.287-12582C>A
XM_011525724.1:c.287-12582C>A	XP_011524026.1:n.287-12582C>A
XM_011525725.1:c.287-12582C>A	XP_011524027.1:n.287-12582C>A
XM_011525726.1:c.287-12582C>A	XP_011524028.1:n.287-12582C>A
XM_011525727.1:c.287-12582C>A	XP_011524029.1:n.287-12582C>A
XM_011525723.3:c.287-12582C>A	XP_011524025.1:n.287-12582C>A
XM_011525724.3:c.287-12582C>A	XP_011524026.1:n.287-12582C>A
XM_011525725.3:c.287-12582C>A	XP_011524027.1:n.287-12582C>A
XM_011525726.3:c.287-12582C>A	XP_011524028.1:n.287-12582C>A
XM_017025918.2:c.287-12582C>A	XP_016881407.1:n.287-12582C>A
XR_001753259.2:n.1284-12582C>A
NM_001378183.1:c.287-12582C>A MANE Select	NP_001365112.1:n.287-12582C>A
NM_022068.4:c.287-12582C>A	NP_071351.2:n.287-12582C>A