Canonical Allele Identifier: CA401923748

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762605T>A (hg19) ; chr18:g.10762607T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762607T>A , CM000680.2:g.10762607T>A	GRCh38
NC_000018.9:g.10762605T>A , CM000680.1:g.10762605T>A	GRCh37
NC_000018.8:g.10752605T>A	NCBI36
NG_034005.1:g.391156A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3142A>T	ENSP00000372900.4:p.Asn1048Tyr
ENST00000686869.1:n.3199A>T
ENST00000674853.1:c.3142A>T MANE Select	ENSP00000501957.1:p.Asn1048Tyr
ENST00000302079.10:c.3067A>T	ENSP00000303316.6:p.Asn1023Tyr
ENST00000383408.6:c.2920A>T	ENSP00000372900.3:p.Asn974Tyr
ENST00000503781.7:c.3067A>T	ENSP00000421377.3:p.Asn1023Tyr
ENST00000580640.5:c.3142A>T	ENSP00000463094.1:p.Asn1048Tyr
ENST00000582913.5:c.3109A>T	ENSP00000462115.1:p.Asn1037Tyr
NM_022068.3:c.3067A>T	NP_071351.2:p.Asn1023Tyr
XM_011525723.1:c.3199A>T	XP_011524025.1:p.Asn1067Tyr
XM_011525724.1:c.3142A>T	XP_011524026.1:p.Asn1048Tyr
XM_011525725.1:c.3109A>T	XP_011524027.1:p.Asn1037Tyr
XM_011525726.1:c.3199A>T	XP_011524028.1:p.Asn1067Tyr
XM_011525727.1:c.3199A>T	XP_011524029.1:p.Asn1067Tyr
XM_011525723.3:c.3199A>T	XP_011524025.1:p.Asn1067Tyr
XM_011525724.3:c.3142A>T	XP_011524026.1:p.Asn1048Tyr
XM_011525725.3:c.3109A>T	XP_011524027.1:p.Asn1037Tyr
XM_011525726.3:c.3199A>T	XP_011524028.1:p.Asn1067Tyr
XM_017025918.2:c.3160A>T	XP_016881407.1:p.Asn1054Tyr
XR_001753259.2:n.4196A>T
NM_001378183.1:c.3142A>T MANE Select	NP_001365112.1:p.Asn1048Tyr
NM_022068.4:c.3067A>T	NP_071351.2:p.Asn1023Tyr