Canonical Allele Identifier: CA368247488

Gene: PON2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222572.8:c.932C>A MANE Select	ENSP00000222572.3:p.Ser311Tyr
ENST00000222572.7:c.932C>A	ENSP00000222572.3:p.Ser311Tyr
ENST00000433091.6:c.896C>A	ENSP00000404622.2:p.Ser299Tyr
ENST00000446142.5:c.*797C>A	ENSP00000405211.1:n.*797C>A
ENST00000455123.5:c.*219C>A	ENSP00000414515.1:n.*219C>A
ENST00000483292.5:c.514C>A
ENST00000633192.1:c.995C>A	ENSP00000488378.1:p.Ser332Tyr
ENST00000633531.1:c.932C>A	ENSP00000488838.1:p.Ser311Tyr
NM_000305.2:c.932C>A	NP_000296.2:p.Ser311Tyr
NM_001018161.1:c.896C>A	NP_001018171.1:p.Ser299Tyr
XM_005250453.1:c.728C>A	XP_005250510.1:p.Ser243Tyr
XM_005250454.1:c.722C>A	XP_005250511.1:p.Ser241Tyr
XM_011516333.1:c.674C>A	XP_011514635.1:p.Ser225Tyr
XM_017012357.2:c.722C>A	XP_016867846.1:p.Ser241Tyr
XM_017012358.2:c.674C>A	XP_016867847.1:p.Ser225Tyr
NM_000305.3:c.932C>A MANE Select	NP_000296.2:p.Ser311Tyr
NM_001018161.2:c.896C>A	NP_001018171.1:p.Ser299Tyr