Canonical Allele Identifier: CA1727228119
Gene: PON2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95434964G= , CM000669.2:g.95434964G= GRCh38
NC_000007.13:g.95064276G= , CM000669.1:g.95064276G= GRCh37
NC_000007.12:g.94902212G= NCBI36
NG_008725.1:g.5109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222572.8:c.-13C= MANE Select ENSP00000222572.3:n.-13C=
ENST00000222572.7:c.-13C= ENSP00000222572.3:n.-13C=
ENST00000433091.6:c.-13C= ENSP00000404622.2:n.-13C=
ENST00000446142.5:c.-13C= ENSP00000405211.1:n.-13C=
ENST00000455123.5:c.-13C= ENSP00000414515.1:n.-13C=
ENST00000469716.1:n.65C=
ENST00000469926.5:c.-270C= ENSP00000488550.1:n.-270C=
ENST00000471883.1:n.67C=
ENST00000490778.5:c.-325C= ENSP00000488826.1:n.-325C=
ENST00000493290.5:c.-346C= ENSP00000488822.1:n.-346C=
ENST00000632034.1:c.-13C= ENSP00000487898.1:n.-13C=
ENST00000633192.1:c.51C= ENSP00000488378.1:p.Pro17=
ENST00000633531.1:c.-13C= ENSP00000488838.1:n.-13C=
NM_000305.2:c.-13C= NP_000296.2:n.-13C=
NM_001018161.1:c.-13C= NP_001018171.1:n.-13C=
XM_005250453.1:c.-191C= XP_005250510.1:n.-191C=
XM_005250454.1:c.-267C= XP_005250511.1:n.-267C=
XM_011516333.1:c.-341C= XP_011514635.1:n.-341C=
XM_017012357.2:c.-267C= XP_016867846.1:n.-267C=
XM_017012358.2:c.-341C= XP_016867847.1:n.-341C=
NM_000305.3:c.-13C= MANE Select NP_000296.2:n.-13C=
NM_001018161.2:c.-13C= NP_001018171.1:n.-13C=