Canonical Allele Identifier: CA401923520

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762508A>G (hg19) ; chr18:g.10762510A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762510A>G , CM000680.2:g.10762510A>G	GRCh38
NC_000018.9:g.10762508A>G , CM000680.1:g.10762508A>G	GRCh37
NC_000018.8:g.10752508A>G	NCBI36
NG_034005.1:g.391253T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3239T>C	ENSP00000372900.4:p.Val1080Ala
ENST00000686869.1:n.3296T>C
ENST00000674853.1:c.3239T>C MANE Select	ENSP00000501957.1:p.Val1080Ala
ENST00000302079.10:c.3164T>C	ENSP00000303316.6:p.Val1055Ala
ENST00000383408.6:c.3017T>C	ENSP00000372900.3:p.Val1006Ala
ENST00000503781.7:c.3164T>C	ENSP00000421377.3:p.Val1055Ala
ENST00000580640.5:c.3239T>C	ENSP00000463094.1:p.Val1080Ala
ENST00000582913.5:c.3206T>C	ENSP00000462115.1:p.Val1069Ala
NM_022068.3:c.3164T>C	NP_071351.2:p.Val1055Ala
XM_011525723.1:c.3296T>C	XP_011524025.1:p.Val1099Ala
XM_011525724.1:c.3239T>C	XP_011524026.1:p.Val1080Ala
XM_011525725.1:c.3206T>C	XP_011524027.1:p.Val1069Ala
XM_011525726.1:c.3296T>C	XP_011524028.1:p.Val1099Ala
XM_011525727.1:c.3296T>C	XP_011524029.1:p.Val1099Ala
XM_011525723.3:c.3296T>C	XP_011524025.1:p.Val1099Ala
XM_011525724.3:c.3239T>C	XP_011524026.1:p.Val1080Ala
XM_011525725.3:c.3206T>C	XP_011524027.1:p.Val1069Ala
XM_011525726.3:c.3296T>C	XP_011524028.1:p.Val1099Ala
XM_017025918.2:c.3257T>C	XP_016881407.1:p.Val1086Ala
XR_001753259.2:n.4293T>C
NM_001378183.1:c.3239T>C MANE Select	NP_001365112.1:p.Val1080Ala
NM_022068.4:c.3164T>C	NP_071351.2:p.Val1055Ala