Canonical Allele Identifier: CA401923539

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762518G>T (hg19) ; chr18:g.10762520G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762520G>T , CM000680.2:g.10762520G>T	GRCh38
NC_000018.9:g.10762518G>T , CM000680.1:g.10762518G>T	GRCh37
NC_000018.8:g.10752518G>T	NCBI36
NG_034005.1:g.391243C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3229C>A	ENSP00000372900.4:p.Pro1077Thr
ENST00000686869.1:n.3286C>A
ENST00000674853.1:c.3229C>A MANE Select	ENSP00000501957.1:p.Pro1077Thr
ENST00000302079.10:c.3154C>A	ENSP00000303316.6:p.Pro1052Thr
ENST00000383408.6:c.3007C>A	ENSP00000372900.3:p.Pro1003Thr
ENST00000503781.7:c.3154C>A	ENSP00000421377.3:p.Pro1052Thr
ENST00000580640.5:c.3229C>A	ENSP00000463094.1:p.Pro1077Thr
ENST00000582913.5:c.3196C>A	ENSP00000462115.1:p.Pro1066Thr
NM_022068.3:c.3154C>A	NP_071351.2:p.Pro1052Thr
XM_011525723.1:c.3286C>A	XP_011524025.1:p.Pro1096Thr
XM_011525724.1:c.3229C>A	XP_011524026.1:p.Pro1077Thr
XM_011525725.1:c.3196C>A	XP_011524027.1:p.Pro1066Thr
XM_011525726.1:c.3286C>A	XP_011524028.1:p.Pro1096Thr
XM_011525727.1:c.3286C>A	XP_011524029.1:p.Pro1096Thr
XM_011525723.3:c.3286C>A	XP_011524025.1:p.Pro1096Thr
XM_011525724.3:c.3229C>A	XP_011524026.1:p.Pro1077Thr
XM_011525725.3:c.3196C>A	XP_011524027.1:p.Pro1066Thr
XM_011525726.3:c.3286C>A	XP_011524028.1:p.Pro1096Thr
XM_017025918.2:c.3247C>A	XP_016881407.1:p.Pro1083Thr
XR_001753259.2:n.4283C>A
NM_001378183.1:c.3229C>A MANE Select	NP_001365112.1:p.Pro1077Thr
NM_022068.4:c.3154C>A	NP_071351.2:p.Pro1052Thr