Canonical Allele Identifier: CA1727229007

Gene: PON2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95411704G= , CM000669.2:g.95411704G=	GRCh38
NC_000007.13:g.95041016G= , CM000669.1:g.95041016G=	GRCh37
NC_000007.12:g.94878952G=	NCBI36
NG_008725.1:g.28369C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000305.3:c.443C= MANE Select	NP_000296.2:p.Ala148=
ENST00000222572.8:c.443C= MANE Select	ENSP00000222572.3:p.Ala148=
NM_000305.2:c.443C=	NP_000296.2:p.Ala148=
NM_001018161.1:c.407C=	NP_001018171.1:p.Ala136=
NM_001018161.2:c.407C=	NP_001018171.1:p.Ala136=
ENST00000222572.7:c.443C=	ENSP00000222572.3:p.Ala148=
ENST00000433091.6:c.407C=	ENSP00000404622.2:p.Ala136=
ENST00000446142.5:c.*308C=	ENSP00000405211.1:n.*308C=
ENST00000455123.5:c.443C=	ENSP00000414515.1:p.Ala148=
ENST00000469926.5:c.185C=	ENSP00000488550.1:p.Ala62=
ENST00000490778.5:c.185C=	ENSP00000488826.1:p.Ala62=
ENST00000491069.5:c.513C=	ENSP00000488462.1:n.513C=
ENST00000632034.1:c.*258C=	ENSP00000487898.1:n.*258C=
ENST00000633192.1:c.506C=	ENSP00000488378.1:p.Ala169=
ENST00000633531.1:c.443C=	ENSP00000488838.1:p.Ala148=
XM_005250453.1:c.239C=	XP_005250510.1:p.Ala80=
XM_005250454.1:c.233C=	XP_005250511.1:p.Ala78=
XM_011516333.1:c.185C=	XP_011514635.1:p.Ala62=
XM_017012357.2:c.233C=	XP_016867846.1:p.Ala78=
XM_017012358.2:c.185C=	XP_016867847.1:p.Ala62=