Canonical Allele Identifier: CA1727246816

Gene: PON2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95424103A= , CM000669.2:g.95424103A=	GRCh38
NC_000007.13:g.95053415A= , CM000669.1:g.95053415A=	GRCh37
NC_000007.12:g.94891351A=	NCBI36
NG_008725.1:g.15970T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000305.3:c.145+412T= MANE Select	NP_000296.2:n.145+412T=
ENST00000222572.8:c.145+412T= MANE Select	ENSP00000222572.3:n.145+412T=
NM_000305.2:c.145+412T=	NP_000296.2:n.145+412T=
NM_001018161.1:c.145+412T=	NP_001018171.1:n.145+412T=
NM_001018161.2:c.145+412T=	NP_001018171.1:n.145+412T=
ENST00000222572.7:c.145+412T=	ENSP00000222572.3:n.145+412T=
ENST00000433091.6:c.145+412T=	ENSP00000404622.2:n.145+412T=
ENST00000446142.5:c.145+412T=	ENSP00000405211.1:n.145+412T=
ENST00000455123.5:c.145+412T=	ENSP00000414515.1:n.145+412T=
ENST00000460873.5:n.145+412T=
ENST00000469926.5:c.-183-7806T=	ENSP00000488550.1:n.-183-7806T=
ENST00000471883.1:n.224+412T=
ENST00000478801.5:c.-239+412T=	ENSP00000487703.1:n.-239+412T=
ENST00000490778.5:c.-168+412T=	ENSP00000488826.1:n.-168+412T=
ENST00000491069.5:c.145+412T=	ENSP00000488462.1:n.145+412T=
ENST00000493290.5:c.-114+412T=	ENSP00000488822.1:n.-114+412T=
ENST00000493469.5:n.157+412T=
ENST00000632034.1:c.145+412T=	ENSP00000487898.1:n.145+412T=
ENST00000633192.1:c.208+412T=	ENSP00000488378.1:n.208+412T=
ENST00000633531.1:c.145+412T=	ENSP00000488838.1:n.145+412T=
XM_005250453.1:c.-34+412T=	XP_005250510.1:n.-34+412T=
XM_005250454.1:c.-110+412T=	XP_005250511.1:n.-110+412T=
XM_011516333.1:c.-184+412T=	XP_011514635.1:n.-184+412T=
XM_017012357.2:c.-110+412T=	XP_016867846.1:n.-110+412T=
XM_017012358.2:c.-184+412T=	XP_016867847.1:n.-184+412T=