Canonical Allele Identifier: CA2284452607

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762939_10762950delinsAGAAGTTCTCAG , CM000680.2:g.10762939_10762950delinsAGAAGTTCTCAG	GRCh38
NC_000018.9:g.10762937_10762948delinsAGAAGTTCTCAG , CM000680.1:g.10762937_10762948delinsAGAAGTTCTCAG	GRCh37
NC_000018.8:g.10752937_10752948delinsAGAAGTTCTCAG	NCBI36
NG_034005.1:g.390813_390824delinsCTGAGAACTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383408.7:c.3095_3106delinsCTGAGAACTTCT	ENSP00000372900.4:p.Pro1032=
ENST00000686869.1:n.3152_3163delinsCTGAGAACTTCT
ENST00000674853.1:c.3095_3106delinsCTGAGAACTTCT MANE Select	ENSP00000501957.1:p.Pro1032=
ENST00000302079.10:c.3020_3031delinsCTGAGAACTTCT	ENSP00000303316.6:p.Pro1007=
ENST00000383408.6:c.2873_2884delinsCTGAGAACTTCT	ENSP00000372900.3:p.Pro958=
ENST00000503781.7:c.3020_3031delinsCTGAGAACTTCT	ENSP00000421377.3:p.Pro1007=
ENST00000580640.5:c.3095_3106delinsCTGAGAACTTCT	ENSP00000463094.1:p.Pro1032=
ENST00000582913.5:c.3062_3073delinsCTGAGAACTTCT	ENSP00000462115.1:p.Pro1021=
NM_022068.3:c.3020_3031delinsCTGAGAACTTCT	NP_071351.2:p.Pro1007=
XM_011525723.1:c.3152_3163delinsCTGAGAACTTCT	XP_011524025.1:p.Pro1051=
XM_011525724.1:c.3095_3106delinsCTGAGAACTTCT	XP_011524026.1:p.Pro1032=
XM_011525725.1:c.3062_3073delinsCTGAGAACTTCT	XP_011524027.1:p.Pro1021=
XM_011525726.1:c.3152_3163delinsCTGAGAACTTCT	XP_011524028.1:p.Pro1051=
XM_011525727.1:c.3152_3163delinsCTGAGAACTTCT	XP_011524029.1:p.Pro1051=
XM_011525723.3:c.3152_3163delinsCTGAGAACTTCT	XP_011524025.1:p.Pro1051=
XM_011525724.3:c.3095_3106delinsCTGAGAACTTCT	XP_011524026.1:p.Pro1032=
XM_011525725.3:c.3062_3073delinsCTGAGAACTTCT	XP_011524027.1:p.Pro1021=
XM_011525726.3:c.3152_3163delinsCTGAGAACTTCT	XP_011524028.1:p.Pro1051=
XM_017025918.2:c.3113_3124delinsCTGAGAACTTCT	XP_016881407.1:p.Pro1038=
XR_001753259.2:n.4149_4160delinsCTGAGAACTTCT
NM_001378183.1:c.3095_3106delinsCTGAGAACTTCT MANE Select	NP_001365112.1:p.Pro1032=
NM_022068.4:c.3020_3031delinsCTGAGAACTTCT	NP_071351.2:p.Pro1007=