Canonical Allele Identifier: CA2284409265

Gene: PIEZO2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10671571A= , CM000680.2:g.10671571A=	GRCh38
NC_000018.9:g.10671568A= , CM000680.1:g.10671568A=	GRCh37
NC_000018.8:g.10661568A=	NCBI36
NG_034005.1:g.482192T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001378183.1:c.8554T= MANE Select	NP_001365112.1:p.Ser2852=
ENST00000674853.1:c.8554T= MANE Select	ENSP00000501957.1:p.Ser2852=
NM_022068.3:c.8215T=	NP_071351.2:p.Ser2739=
NM_022068.4:c.8215T=	NP_071351.2:p.Ser2739=
ENST00000302079.10:c.8026T=	ENSP00000303316.6:p.Ser2676=
ENST00000383408.6:c.8068T=	ENSP00000372900.3:p.Ser2690=
ENST00000383408.7:c.*1656T=	ENSP00000372900.4:n.*1656T=
ENST00000503781.7:c.8215T=	ENSP00000421377.3:p.Ser2739=
ENST00000538948.5:c.2086T=	ENSP00000443129.1:p.Ser696=
ENST00000580640.5:c.8290T=	ENSP00000463094.1:p.Ser2764=
ENST00000582913.5:c.8421T=	ENSP00000462115.1:n.8421T=
ENST00000582937.1:c.58+1119T=	ENSP00000462187.1:n.58+1119T=
ENST00000685517.1:n.3297T=
ENST00000691469.1:n.2452T=
ENST00000693743.1:c.1750T=	ENSP00000510331.1:n.1750T=
XM_011525723.1:c.8347T=	XP_011524025.1:p.Ser2783=
XM_011525723.3:c.8347T=	XP_011524025.1:p.Ser2783=
XM_011525724.1:c.8290T=	XP_011524026.1:p.Ser2764=
XM_011525724.3:c.8290T=	XP_011524026.1:p.Ser2764=
XM_011525725.1:c.8257T=	XP_011524027.1:p.Ser2753=
XM_011525725.3:c.8257T=	XP_011524027.1:p.Ser2753=
XM_011525726.1:c.8164T=	XP_011524028.1:p.Ser2722=
XM_011525726.3:c.8164T=	XP_011524028.1:p.Ser2722=
XM_017025918.2:c.8308T=	XP_016881407.1:p.Ser2770=