Canonical Allele Identifier: CA502900491

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762609T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762611T>C , CM000680.2:g.10762611T>C	GRCh38
NC_000018.9:g.10762609T>C , CM000680.1:g.10762609T>C	GRCh37
NC_000018.8:g.10752609T>C	NCBI36
NG_034005.1:g.391152A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3138A>G	ENSP00000372900.4:p.Gln1046=
ENST00000686869.1:n.3195A>G
ENST00000674853.1:c.3138A>G MANE Select	ENSP00000501957.1:p.Gln1046=
ENST00000302079.10:c.3063A>G	ENSP00000303316.6:p.Gln1021=
ENST00000383408.6:c.2916A>G	ENSP00000372900.3:p.Gln972=
ENST00000503781.7:c.3063A>G	ENSP00000421377.3:p.Gln1021=
ENST00000580640.5:c.3138A>G	ENSP00000463094.1:p.Gln1046=
ENST00000582913.5:c.3105A>G	ENSP00000462115.1:p.Gln1035=
NM_022068.3:c.3063A>G	NP_071351.2:p.Gln1021=
XM_011525723.1:c.3195A>G	XP_011524025.1:p.Gln1065=
XM_011525724.1:c.3138A>G	XP_011524026.1:p.Gln1046=
XM_011525725.1:c.3105A>G	XP_011524027.1:p.Gln1035=
XM_011525726.1:c.3195A>G	XP_011524028.1:p.Gln1065=
XM_011525727.1:c.3195A>G	XP_011524029.1:p.Gln1065=
XM_011525723.3:c.3195A>G	XP_011524025.1:p.Gln1065=
XM_011525724.3:c.3138A>G	XP_011524026.1:p.Gln1046=
XM_011525725.3:c.3105A>G	XP_011524027.1:p.Gln1035=
XM_011525726.3:c.3195A>G	XP_011524028.1:p.Gln1065=
XM_017025918.2:c.3156A>G	XP_016881407.1:p.Gln1052=
XR_001753259.2:n.4192A>G
NM_001378183.1:c.3138A>G MANE Select	NP_001365112.1:p.Gln1046=
NM_022068.4:c.3063A>G	NP_071351.2:p.Gln1021=