Canonical Allele Identifier: CA401923813

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762619T>C (hg19) ; chr18:g.10762621T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762621T>C , CM000680.2:g.10762621T>C	GRCh38
NC_000018.9:g.10762619T>C , CM000680.1:g.10762619T>C	GRCh37
NC_000018.8:g.10752619T>C	NCBI36
NG_034005.1:g.391142A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3128A>G	ENSP00000372900.4:p.Asn1043Ser
ENST00000686869.1:n.3185A>G
ENST00000674853.1:c.3128A>G MANE Select	ENSP00000501957.1:p.Asn1043Ser
ENST00000302079.10:c.3053A>G	ENSP00000303316.6:p.Asn1018Ser
ENST00000383408.6:c.2906A>G	ENSP00000372900.3:p.Asn969Ser
ENST00000503781.7:c.3053A>G	ENSP00000421377.3:p.Asn1018Ser
ENST00000580640.5:c.3128A>G	ENSP00000463094.1:p.Asn1043Ser
ENST00000582913.5:c.3095A>G	ENSP00000462115.1:p.Asn1032Ser
NM_022068.3:c.3053A>G	NP_071351.2:p.Asn1018Ser
XM_011525723.1:c.3185A>G	XP_011524025.1:p.Asn1062Ser
XM_011525724.1:c.3128A>G	XP_011524026.1:p.Asn1043Ser
XM_011525725.1:c.3095A>G	XP_011524027.1:p.Asn1032Ser
XM_011525726.1:c.3185A>G	XP_011524028.1:p.Asn1062Ser
XM_011525727.1:c.3185A>G	XP_011524029.1:p.Asn1062Ser
XM_011525723.3:c.3185A>G	XP_011524025.1:p.Asn1062Ser
XM_011525724.3:c.3128A>G	XP_011524026.1:p.Asn1043Ser
XM_011525725.3:c.3095A>G	XP_011524027.1:p.Asn1032Ser
XM_011525726.3:c.3185A>G	XP_011524028.1:p.Asn1062Ser
XM_017025918.2:c.3146A>G	XP_016881407.1:p.Asn1049Ser
XR_001753259.2:n.4182A>G
NM_001378183.1:c.3128A>G MANE Select	NP_001365112.1:p.Asn1043Ser
NM_022068.4:c.3053A>G	NP_071351.2:p.Asn1018Ser