Canonical Allele Identifier: CA1727254038

Gene: PON2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95405463G= , CM000669.2:g.95405463G=	GRCh38
NC_000007.13:g.95034775G= , CM000669.1:g.95034775G=	GRCh37
NC_000007.12:g.94872711G=	NCBI36
NG_008725.1:g.34610C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000305.3:c.932C= MANE Select	NP_000296.2:p.Ser311=
ENST00000222572.8:c.932C= MANE Select	ENSP00000222572.3:p.Ser311=
NM_000305.2:c.932C=	NP_000296.2:p.Ser311=
NM_001018161.1:c.896C=	NP_001018171.1:p.Ser299=
NM_001018161.2:c.896C=	NP_001018171.1:p.Ser299=
ENST00000222572.7:c.932C=	ENSP00000222572.3:p.Ser311=
ENST00000433091.6:c.896C=	ENSP00000404622.2:p.Ser299=
ENST00000446142.5:c.*797C=	ENSP00000405211.1:n.*797C=
ENST00000455123.5:c.*219C=	ENSP00000414515.1:n.*219C=
ENST00000483292.5:c.514C=
ENST00000633192.1:c.995C=	ENSP00000488378.1:p.Ser332=
ENST00000633531.1:c.932C=	ENSP00000488838.1:p.Ser311=
XM_005250453.1:c.728C=	XP_005250510.1:p.Ser243=
XM_005250454.1:c.722C=	XP_005250511.1:p.Ser241=
XM_011516333.1:c.674C=	XP_011514635.1:p.Ser225=
XM_017012357.2:c.722C=	XP_016867846.1:p.Ser241=
XM_017012358.2:c.674C=	XP_016867847.1:p.Ser225=