Canonical Allele Identifier: CA2284425174
Gene: PIEZO2 HGNC NCBI

Linked Data

dbSNP Id: rs2035526961

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10705250_10705251dup , CM000680.2:g.10705250_10705251dup GRCh38
NC_000018.9:g.10705248_10705249dup , CM000680.1:g.10705248_10705249dup GRCh37
NC_000018.8:g.10695248_10695249dup NCBI36
NG_034005.1:g.448517_448518dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.5735+90_5735+91dup ENSP00000372900.4:n.5735+90_5735+91dup
ENST00000674853.1:c.5999+90_5999+91dup MANE Select ENSP00000501957.1:n.5999+90_5999+91dup
ENST00000302079.10:c.5660+90_5660+91dup ENSP00000303316.6:n.5660+90_5660+91dup
ENST00000383408.6:c.5513+90_5513+91dup ENSP00000372900.3:n.5513+90_5513+91dup
ENST00000503781.7:c.5660+90_5660+91dup ENSP00000421377.3:n.5660+90_5660+91dup
ENST00000580640.5:c.5735+90_5735+91dup ENSP00000463094.1:n.5735+90_5735+91dup
ENST00000582913.5:c.5866+90_5866+91dup ENSP00000462115.1:n.5866+90_5866+91dup
NM_022068.3:c.5660+90_5660+91dup NP_071351.2:n.5660+90_5660+91dup
XM_011525723.1:c.5792+90_5792+91dup XP_011524025.1:n.5792+90_5792+91dup
XM_011525724.1:c.5735+90_5735+91dup XP_011524026.1:n.5735+90_5735+91dup
XM_011525725.1:c.5702+90_5702+91dup XP_011524027.1:n.5702+90_5702+91dup
XM_011525726.1:c.5792+90_5792+91dup XP_011524028.1:n.5792+90_5792+91dup
XM_011525723.3:c.5792+90_5792+91dup XP_011524025.1:n.5792+90_5792+91dup
XM_011525724.3:c.5735+90_5735+91dup XP_011524026.1:n.5735+90_5735+91dup
XM_011525725.3:c.5702+90_5702+91dup XP_011524027.1:n.5702+90_5702+91dup
XM_011525726.3:c.5792+90_5792+91dup XP_011524028.1:n.5792+90_5792+91dup
XM_017025918.2:c.5753+90_5753+91dup XP_016881407.1:n.5753+90_5753+91dup
XR_001753259.2:n.6789+90_6789+91dup
NM_001378183.1:c.5999+90_5999+91dup MANE Select NP_001365112.1:n.5999+90_5999+91dup
NM_022068.4:c.5660+90_5660+91dup NP_071351.2:n.5660+90_5660+91dup