Canonical Allele Identifier: CA502900364

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762513C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762515C>A , CM000680.2:g.10762515C>A	GRCh38
NC_000018.9:g.10762513C>A , CM000680.1:g.10762513C>A	GRCh37
NC_000018.8:g.10752513C>A	NCBI36
NG_034005.1:g.391248G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3234G>T	ENSP00000372900.4:p.Leu1078=
ENST00000686869.1:n.3291G>T
ENST00000674853.1:c.3234G>T MANE Select	ENSP00000501957.1:p.Leu1078=
ENST00000302079.10:c.3159G>T	ENSP00000303316.6:p.Leu1053=
ENST00000383408.6:c.3012G>T	ENSP00000372900.3:p.Leu1004=
ENST00000503781.7:c.3159G>T	ENSP00000421377.3:p.Leu1053=
ENST00000580640.5:c.3234G>T	ENSP00000463094.1:p.Leu1078=
ENST00000582913.5:c.3201G>T	ENSP00000462115.1:p.Leu1067=
NM_022068.3:c.3159G>T	NP_071351.2:p.Leu1053=
XM_011525723.1:c.3291G>T	XP_011524025.1:p.Leu1097=
XM_011525724.1:c.3234G>T	XP_011524026.1:p.Leu1078=
XM_011525725.1:c.3201G>T	XP_011524027.1:p.Leu1067=
XM_011525726.1:c.3291G>T	XP_011524028.1:p.Leu1097=
XM_011525727.1:c.3291G>T	XP_011524029.1:p.Leu1097=
XM_011525723.3:c.3291G>T	XP_011524025.1:p.Leu1097=
XM_011525724.3:c.3234G>T	XP_011524026.1:p.Leu1078=
XM_011525725.3:c.3201G>T	XP_011524027.1:p.Leu1067=
XM_011525726.3:c.3291G>T	XP_011524028.1:p.Leu1097=
XM_017025918.2:c.3252G>T	XP_016881407.1:p.Leu1084=
XR_001753259.2:n.4288G>T
NM_001378183.1:c.3234G>T MANE Select	NP_001365112.1:p.Leu1078=
NM_022068.4:c.3159G>T	NP_071351.2:p.Leu1053=