Canonical Allele Identifier: CA401923824
Gene: PIEZO2 HGNC NCBI

Linked Data

dbSNP Id: rs557288488

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10762624G>C , CM000680.2:g.10762624G>C GRCh38
NC_000018.9:g.10762622G>C , CM000680.1:g.10762622G>C GRCh37
NC_000018.8:g.10752622G>C NCBI36
NG_034005.1:g.391139C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.3125C>G ENSP00000372900.4:p.Pro1042Arg
ENST00000686869.1:n.3182C>G
ENST00000674853.1:c.3125C>G MANE Select ENSP00000501957.1:p.Pro1042Arg
ENST00000302079.10:c.3050C>G ENSP00000303316.6:p.Pro1017Arg
ENST00000383408.6:c.2903C>G ENSP00000372900.3:p.Pro968Arg
ENST00000503781.7:c.3050C>G ENSP00000421377.3:p.Pro1017Arg
ENST00000580640.5:c.3125C>G ENSP00000463094.1:p.Pro1042Arg
ENST00000582913.5:c.3092C>G ENSP00000462115.1:p.Pro1031Arg
NM_022068.3:c.3050C>G NP_071351.2:p.Pro1017Arg
XM_011525723.1:c.3182C>G XP_011524025.1:p.Pro1061Arg
XM_011525724.1:c.3125C>G XP_011524026.1:p.Pro1042Arg
XM_011525725.1:c.3092C>G XP_011524027.1:p.Pro1031Arg
XM_011525726.1:c.3182C>G XP_011524028.1:p.Pro1061Arg
XM_011525727.1:c.3182C>G XP_011524029.1:p.Pro1061Arg
XM_011525723.3:c.3182C>G XP_011524025.1:p.Pro1061Arg
XM_011525724.3:c.3125C>G XP_011524026.1:p.Pro1042Arg
XM_011525725.3:c.3092C>G XP_011524027.1:p.Pro1031Arg
XM_011525726.3:c.3182C>G XP_011524028.1:p.Pro1061Arg
XM_017025918.2:c.3143C>G XP_016881407.1:p.Pro1048Arg
XR_001753259.2:n.4179C>G
NM_001378183.1:c.3125C>G MANE Select NP_001365112.1:p.Pro1042Arg
NM_022068.4:c.3050C>G NP_071351.2:p.Pro1017Arg