Canonical Allele Identifier: CA2810962563

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10784974_10784975insCACACCCAAC , CM000680.2:g.10784974_10784975insCACACCCAAC	GRCh38
NC_000018.9:g.10784972_10784973insCACACCCAAC , CM000680.1:g.10784972_10784973insCACACCCAAC	GRCh37
NC_000018.8:g.10774972_10774973insCACACCCAAC	NCBI36
NG_034005.1:g.368788_368789insGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.2319-18_2319-17insGTTGGGTGTG	ENSP00000372900.4:n.2319-18_2319-17insGTTGGGTGTG
ENST00000686869.1:n.2376-18_2376-17insGTTGGGTGTG
ENST00000674853.1:c.2319-18_2319-17insGTTGGGTGTG MANE Select	ENSP00000501957.1:n.2319-18_2319-17insGTTGGGTGTG
ENST00000302079.10:c.2319-18_2319-17insGTTGGGTGTG	ENSP00000303316.6:n.2319-18_2319-17insGTTGGGTGTG
ENST00000383408.6:c.2166-18_2166-17insGTTGGGTGTG	ENSP00000372900.3:n.2166-18_2166-17insGTTGGGTGTG
ENST00000503781.7:c.2319-18_2319-17insGTTGGGTGTG	ENSP00000421377.3:n.2319-18_2319-17insGTTGGGTGTG
ENST00000580640.5:c.2319-18_2319-17insGTTGGGTGTG	ENSP00000463094.1:n.2319-18_2319-17insGTTGGGTGTG
ENST00000582913.5:c.2319-18_2319-17insGTTGGGTGTG	ENSP00000462115.1:n.2319-18_2319-17insGTTGGGTGTG
ENST00000583325.1:c.306-18_306-17insGTTGGGTGTG	ENSP00000462560.1:n.306-18_306-17insGTTGGGTGTG
NM_022068.3:c.2319-18_2319-17insGTTGGGTGTG	NP_071351.2:n.2319-18_2319-17insGTTGGGTGTG
XM_011525723.1:c.2319-18_2319-17insGTTGGGTGTG	XP_011524025.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525724.1:c.2319-18_2319-17insGTTGGGTGTG	XP_011524026.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525725.1:c.2319-18_2319-17insGTTGGGTGTG	XP_011524027.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525726.1:c.2319-18_2319-17insGTTGGGTGTG	XP_011524028.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525727.1:c.2319-18_2319-17insGTTGGGTGTG	XP_011524029.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525723.3:c.2319-18_2319-17insGTTGGGTGTG	XP_011524025.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525724.3:c.2319-18_2319-17insGTTGGGTGTG	XP_011524026.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525725.3:c.2319-18_2319-17insGTTGGGTGTG	XP_011524027.1:n.2319-18_2319-17insGTTGGGTGTG
XM_011525726.3:c.2319-18_2319-17insGTTGGGTGTG	XP_011524028.1:n.2319-18_2319-17insGTTGGGTGTG
XM_017025918.2:c.2280-18_2280-17insGTTGGGTGTG	XP_016881407.1:n.2280-18_2280-17insGTTGGGTGTG
XR_001753259.2:n.3316-18_3316-17insGTTGGGTGTG
NM_001378183.1:c.2319-18_2319-17insGTTGGGTGTG MANE Select	NP_001365112.1:n.2319-18_2319-17insGTTGGGTGTG
NM_022068.4:c.2319-18_2319-17insGTTGGGTGTG	NP_071351.2:n.2319-18_2319-17insGTTGGGTGTG