Canonical Allele Identifier: CA502900395

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762549A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762551A>G , CM000680.2:g.10762551A>G	GRCh38
NC_000018.9:g.10762549A>G , CM000680.1:g.10762549A>G	GRCh37
NC_000018.8:g.10752549A>G	NCBI36
NG_034005.1:g.391212T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3198T>C	ENSP00000372900.4:p.Pro1066=
ENST00000686869.1:n.3255T>C
ENST00000674853.1:c.3198T>C MANE Select	ENSP00000501957.1:p.Pro1066=
ENST00000302079.10:c.3123T>C	ENSP00000303316.6:p.Pro1041=
ENST00000383408.6:c.2976T>C	ENSP00000372900.3:p.Pro992=
ENST00000503781.7:c.3123T>C	ENSP00000421377.3:p.Pro1041=
ENST00000580640.5:c.3198T>C	ENSP00000463094.1:p.Pro1066=
ENST00000582913.5:c.3165T>C	ENSP00000462115.1:p.Pro1055=
NM_022068.3:c.3123T>C	NP_071351.2:p.Pro1041=
XM_011525723.1:c.3255T>C	XP_011524025.1:p.Pro1085=
XM_011525724.1:c.3198T>C	XP_011524026.1:p.Pro1066=
XM_011525725.1:c.3165T>C	XP_011524027.1:p.Pro1055=
XM_011525726.1:c.3255T>C	XP_011524028.1:p.Pro1085=
XM_011525727.1:c.3255T>C	XP_011524029.1:p.Pro1085=
XM_011525723.3:c.3255T>C	XP_011524025.1:p.Pro1085=
XM_011525724.3:c.3198T>C	XP_011524026.1:p.Pro1066=
XM_011525725.3:c.3165T>C	XP_011524027.1:p.Pro1055=
XM_011525726.3:c.3255T>C	XP_011524028.1:p.Pro1085=
XM_017025918.2:c.3216T>C	XP_016881407.1:p.Pro1072=
XR_001753259.2:n.4252T>C
NM_001378183.1:c.3198T>C MANE Select	NP_001365112.1:p.Pro1066=
NM_022068.4:c.3123T>C	NP_071351.2:p.Pro1041=