Canonical Allele Identifier: CA378980017
Gene: PNPLA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.822419C>A , CM000673.2:g.822419C>A GRCh38
NC_000011.9:g.822419C>A , CM000673.1:g.822419C>A GRCh37
NC_000011.8:g.812419C>A NCBI36
NG_023394.1:g.8519C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336615.9:c.509C>A MANE Select ENSP00000337701.4:p.Ser170Ter
ENST00000336615.8:c.509C>A ENSP00000337701.4:p.Ser170Ter
ENST00000525250.5:n.1115C>A
ENST00000531923.1:n.404C>A
ENST00000617551.1:c.-742C>A ENSP00000481602.1:n.-742C>A
NM_020376.3:c.509C>A NP_065109.1:p.Ser170Ter
XM_006718265.2:c.509C>A XP_006718328.1:p.Ser170Ter
XM_006718266.2:c.509C>A XP_006718329.1:p.Ser170Ter
XM_006718265.3:c.509C>A XP_006718328.1:p.Ser170Ter
XM_006718266.3:c.509C>A XP_006718329.1:p.Ser170Ter
XM_017018028.1:c.509C>A XP_016873517.1:p.Ser170Ter
XM_024448618.1:c.509C>A XP_024304386.1:p.Ser170Ter
NM_020376.4:c.509C>A MANE Select NP_065109.1:p.Ser170Ter