Canonical Allele Identifier: CA401920162

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10784780A>G (hg19) ; chr18:g.10784782A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10784782A>G , CM000680.2:g.10784782A>G	GRCh38
NC_000018.9:g.10784780A>G , CM000680.1:g.10784780A>G	GRCh37
NC_000018.8:g.10774780A>G	NCBI36
NG_034005.1:g.368981T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.2492+2T>C	ENSP00000372900.4:n.2492+2T>C
ENST00000686869.1:n.2549+2T>C
ENST00000674853.1:c.2492+2T>C MANE Select	ENSP00000501957.1:n.2492+2T>C
ENST00000302079.10:c.2492+2T>C	ENSP00000303316.6:n.2492+2T>C
ENST00000383408.6:c.2339+2T>C	ENSP00000372900.3:n.2339+2T>C
ENST00000503781.7:c.2492+2T>C	ENSP00000421377.3:n.2492+2T>C
ENST00000580640.5:c.2492+2T>C	ENSP00000463094.1:n.2492+2T>C
ENST00000582913.5:c.2492+2T>C	ENSP00000462115.1:n.2492+2T>C
ENST00000583325.1:c.479+2T>C	ENSP00000462560.1:n.479+2T>C
NM_022068.3:c.2492+2T>C	NP_071351.2:n.2492+2T>C
XM_011525723.1:c.2492+2T>C	XP_011524025.1:n.2492+2T>C
XM_011525724.1:c.2492+2T>C	XP_011524026.1:n.2492+2T>C
XM_011525725.1:c.2492+2T>C	XP_011524027.1:n.2492+2T>C
XM_011525726.1:c.2492+2T>C	XP_011524028.1:n.2492+2T>C
XM_011525727.1:c.2492+2T>C	XP_011524029.1:n.2492+2T>C
XM_011525723.3:c.2492+2T>C	XP_011524025.1:n.2492+2T>C
XM_011525724.3:c.2492+2T>C	XP_011524026.1:n.2492+2T>C
XM_011525725.3:c.2492+2T>C	XP_011524027.1:n.2492+2T>C
XM_011525726.3:c.2492+2T>C	XP_011524028.1:n.2492+2T>C
XM_017025918.2:c.2453+2T>C	XP_016881407.1:n.2453+2T>C
XR_001753259.2:n.3489+2T>C
NM_001378183.1:c.2492+2T>C MANE Select	NP_001365112.1:n.2492+2T>C
NM_022068.4:c.2492+2T>C	NP_071351.2:n.2492+2T>C