Canonical Allele Identifier: CA502900368

Gene: PIEZO2

Linked Data

• MyVariant Identifiers: chr18:g.10762516A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762518A>T , CM000680.2:g.10762518A>T	GRCh38
NC_000018.9:g.10762516A>T , CM000680.1:g.10762516A>T	GRCh37
NC_000018.8:g.10752516A>T	NCBI36
NG_034005.1:g.391245T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3231T>A	ENSP00000372900.4:p.Pro1077=
ENST00000686869.1:n.3288T>A
ENST00000674853.1:c.3231T>A MANE Select	ENSP00000501957.1:p.Pro1077=
ENST00000302079.10:c.3156T>A	ENSP00000303316.6:p.Pro1052=
ENST00000383408.6:c.3009T>A	ENSP00000372900.3:p.Pro1003=
ENST00000503781.7:c.3156T>A	ENSP00000421377.3:p.Pro1052=
ENST00000580640.5:c.3231T>A	ENSP00000463094.1:p.Pro1077=
ENST00000582913.5:c.3198T>A	ENSP00000462115.1:p.Pro1066=
NM_022068.3:c.3156T>A	NP_071351.2:p.Pro1052=
XM_011525723.1:c.3288T>A	XP_011524025.1:p.Pro1096=
XM_011525724.1:c.3231T>A	XP_011524026.1:p.Pro1077=
XM_011525725.1:c.3198T>A	XP_011524027.1:p.Pro1066=
XM_011525726.1:c.3288T>A	XP_011524028.1:p.Pro1096=
XM_011525727.1:c.3288T>A	XP_011524029.1:p.Pro1096=
XM_011525723.3:c.3288T>A	XP_011524025.1:p.Pro1096=
XM_011525724.3:c.3231T>A	XP_011524026.1:p.Pro1077=
XM_011525725.3:c.3198T>A	XP_011524027.1:p.Pro1066=
XM_011525726.3:c.3288T>A	XP_011524028.1:p.Pro1096=
XM_017025918.2:c.3249T>A	XP_016881407.1:p.Pro1083=
XR_001753259.2:n.4285T>A
NM_001378183.1:c.3231T>A MANE Select	NP_001365112.1:p.Pro1077=
NM_022068.4:c.3156T>A	NP_071351.2:p.Pro1052=