Canonical Allele Identifier: CA1947314845
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.821949G= , CM000673.2:g.821949G= GRCh38
NC_000011.9:g.821949G= , CM000673.1:g.821949G= GRCh37
NC_000011.8:g.811949G= NCBI36
NG_023394.1:g.8049G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336615.9:c.421-9G= MANE Select ENSP00000337701.4:n.421-9G=
ENST00000336615.8:c.421-9G= ENSP00000337701.4:n.421-9G=
ENST00000525250.5:n.1027-9G=
ENST00000534561.1:n.88-9G=
ENST00000617551.1:c.-830-9G= ENSP00000481602.1:n.-830-9G=
NM_020376.3:c.421-9G= NP_065109.1:n.421-9G=
XM_006718265.2:c.421-9G= XP_006718328.1:n.421-9G=
XM_006718266.2:c.421-9G= XP_006718329.1:n.421-9G=
XM_006718265.3:c.421-9G= XP_006718328.1:n.421-9G=
XM_006718266.3:c.421-9G= XP_006718329.1:n.421-9G=
XM_017018028.1:c.421-9G= XP_016873517.1:n.421-9G=
XM_024448618.1:c.421-9G= XP_024304386.1:n.421-9G=
NM_020376.4:c.421-9G= MANE Select NP_065109.1:n.421-9G=