Canonical Allele Identifier: CA502900391
Gene: PIEZO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.10762543C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10762545C>T , CM000680.2:g.10762545C>T GRCh38
NC_000018.9:g.10762543C>T , CM000680.1:g.10762543C>T GRCh37
NC_000018.8:g.10752543C>T NCBI36
NG_034005.1:g.391218G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.3204G>A ENSP00000372900.4:p.Glu1068=
ENST00000686869.1:n.3261G>A
ENST00000674853.1:c.3204G>A MANE Select ENSP00000501957.1:p.Glu1068=
ENST00000302079.10:c.3129G>A ENSP00000303316.6:p.Glu1043=
ENST00000383408.6:c.2982G>A ENSP00000372900.3:p.Glu994=
ENST00000503781.7:c.3129G>A ENSP00000421377.3:p.Glu1043=
ENST00000580640.5:c.3204G>A ENSP00000463094.1:p.Glu1068=
ENST00000582913.5:c.3171G>A ENSP00000462115.1:p.Glu1057=
NM_022068.3:c.3129G>A NP_071351.2:p.Glu1043=
XM_011525723.1:c.3261G>A XP_011524025.1:p.Glu1087=
XM_011525724.1:c.3204G>A XP_011524026.1:p.Glu1068=
XM_011525725.1:c.3171G>A XP_011524027.1:p.Glu1057=
XM_011525726.1:c.3261G>A XP_011524028.1:p.Glu1087=
XM_011525727.1:c.3261G>A XP_011524029.1:p.Glu1087=
XM_011525723.3:c.3261G>A XP_011524025.1:p.Glu1087=
XM_011525724.3:c.3204G>A XP_011524026.1:p.Glu1068=
XM_011525725.3:c.3171G>A XP_011524027.1:p.Glu1057=
XM_011525726.3:c.3261G>A XP_011524028.1:p.Glu1087=
XM_017025918.2:c.3222G>A XP_016881407.1:p.Glu1074=
XR_001753259.2:n.4258G>A
NM_001378183.1:c.3204G>A MANE Select NP_001365112.1:p.Glu1068=
NM_022068.4:c.3129G>A NP_071351.2:p.Glu1043=