Canonical Allele Identifier: CA1947314874
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.821970A= , CM000673.2:g.821970A= GRCh38
NC_000011.9:g.821970A= , CM000673.1:g.821970A= GRCh37
NC_000011.8:g.811970A= NCBI36
NG_023394.1:g.8070A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336615.9:c.433A= MANE Select ENSP00000337701.4:p.Ser145=
ENST00000336615.8:c.433A= ENSP00000337701.4:p.Ser145=
ENST00000525250.5:n.1039A=
ENST00000534561.1:n.100A=
ENST00000617551.1:c.-818A= ENSP00000481602.1:n.-818A=
NM_020376.3:c.433A= NP_065109.1:p.Ser145=
XM_006718265.2:c.433A= XP_006718328.1:p.Ser145=
XM_006718266.2:c.433A= XP_006718329.1:p.Ser145=
XM_006718265.3:c.433A= XP_006718328.1:p.Ser145=
XM_006718266.3:c.433A= XP_006718329.1:p.Ser145=
XM_017018028.1:c.433A= XP_016873517.1:p.Ser145=
XM_024448618.1:c.433A= XP_024304386.1:p.Ser145=
NM_020376.4:c.433A= MANE Select NP_065109.1:p.Ser145=