Canonical Allele Identifier: CA2284452450

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762600G= , CM000680.2:g.10762600G=	GRCh38
NC_000018.9:g.10762598G= , CM000680.1:g.10762598G=	GRCh37
NC_000018.8:g.10752598G=	NCBI36
NG_034005.1:g.391163C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3149C=	ENSP00000372900.4:p.Pro1050=
ENST00000686869.1:n.3206C=
ENST00000674853.1:c.3149C= MANE Select	ENSP00000501957.1:p.Pro1050=
ENST00000302079.10:c.3074C=	ENSP00000303316.6:p.Pro1025=
ENST00000383408.6:c.2927C=	ENSP00000372900.3:p.Pro976=
ENST00000503781.7:c.3074C=	ENSP00000421377.3:p.Pro1025=
ENST00000580640.5:c.3149C=	ENSP00000463094.1:p.Pro1050=
ENST00000582913.5:c.3116C=	ENSP00000462115.1:p.Pro1039=
NM_022068.3:c.3074C=	NP_071351.2:p.Pro1025=
XM_011525723.1:c.3206C=	XP_011524025.1:p.Pro1069=
XM_011525724.1:c.3149C=	XP_011524026.1:p.Pro1050=
XM_011525725.1:c.3116C=	XP_011524027.1:p.Pro1039=
XM_011525726.1:c.3206C=	XP_011524028.1:p.Pro1069=
XM_011525727.1:c.3206C=	XP_011524029.1:p.Pro1069=
XM_011525723.3:c.3206C=	XP_011524025.1:p.Pro1069=
XM_011525724.3:c.3149C=	XP_011524026.1:p.Pro1050=
XM_011525725.3:c.3116C=	XP_011524027.1:p.Pro1039=
XM_011525726.3:c.3206C=	XP_011524028.1:p.Pro1069=
XM_017025918.2:c.3167C=	XP_016881407.1:p.Pro1056=
XR_001753259.2:n.4203C=
NM_001378183.1:c.3149C= MANE Select	NP_001365112.1:p.Pro1050=
NM_022068.4:c.3074C=	NP_071351.2:p.Pro1025=