Canonical Allele Identifier: CA2284452569

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762850G= , CM000680.2:g.10762850G=	GRCh38
NC_000018.9:g.10762848G= , CM000680.1:g.10762848G=	GRCh37
NC_000018.8:g.10752848G=	NCBI36
NG_034005.1:g.390913C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.3123+72C=	ENSP00000372900.4:n.3123+72C=
ENST00000686869.1:n.3180+72C=
ENST00000674853.1:c.3123+72C= MANE Select	ENSP00000501957.1:n.3123+72C=
ENST00000302079.10:c.3048+72C=	ENSP00000303316.6:n.3048+72C=
ENST00000383408.6:c.2901+72C=	ENSP00000372900.3:n.2901+72C=
ENST00000503781.7:c.3048+72C=	ENSP00000421377.3:n.3048+72C=
ENST00000580640.5:c.3123+72C=	ENSP00000463094.1:n.3123+72C=
ENST00000582913.5:c.3090+72C=	ENSP00000462115.1:n.3090+72C=
NM_022068.3:c.3048+72C=	NP_071351.2:n.3048+72C=
XM_011525723.1:c.3180+72C=	XP_011524025.1:n.3180+72C=
XM_011525724.1:c.3123+72C=	XP_011524026.1:n.3123+72C=
XM_011525725.1:c.3090+72C=	XP_011524027.1:n.3090+72C=
XM_011525726.1:c.3180+72C=	XP_011524028.1:n.3180+72C=
XM_011525727.1:c.3180+72C=	XP_011524029.1:n.3180+72C=
XM_011525723.3:c.3180+72C=	XP_011524025.1:n.3180+72C=
XM_011525724.3:c.3123+72C=	XP_011524026.1:n.3123+72C=
XM_011525725.3:c.3090+72C=	XP_011524027.1:n.3090+72C=
XM_011525726.3:c.3180+72C=	XP_011524028.1:n.3180+72C=
XM_017025918.2:c.3141+72C=	XP_016881407.1:n.3141+72C=
XR_001753259.2:n.4177+72C=
NM_001378183.1:c.3123+72C= MANE Select	NP_001365112.1:n.3123+72C=
NM_022068.4:c.3048+72C=	NP_071351.2:n.3048+72C=