Canonical Allele Identifier: CA1947314912
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.821992G= , CM000673.2:g.821992G= GRCh38
NC_000011.9:g.821992G= , CM000673.1:g.821992G= GRCh37
NC_000011.8:g.811992G= NCBI36
NG_023394.1:g.8092G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336615.9:c.455G= MANE Select ENSP00000337701.4:p.Cys152=
ENST00000336615.8:c.455G= ENSP00000337701.4:p.Cys152=
ENST00000525250.5:n.1061G=
ENST00000534561.1:n.122G=
ENST00000617551.1:c.-796G= ENSP00000481602.1:n.-796G=
NM_020376.3:c.455G= NP_065109.1:p.Cys152=
XM_006718265.2:c.455G= XP_006718328.1:p.Cys152=
XM_006718266.2:c.455G= XP_006718329.1:p.Cys152=
XM_006718265.3:c.455G= XP_006718328.1:p.Cys152=
XM_006718266.3:c.455G= XP_006718329.1:p.Cys152=
XM_017018028.1:c.455G= XP_016873517.1:p.Cys152=
XM_024448618.1:c.455G= XP_024304386.1:p.Cys152=
NM_020376.4:c.455G= MANE Select NP_065109.1:p.Cys152=