Canonical Allele Identifier: CA5790908
Community Standard Title: NM_020376.4(PNPLA2):c.165G>T (p.Ala55=)
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.819883G>T , CM000673.2:g.819883G>T GRCh38
NC_000011.9:g.819883G>T , CM000673.1:g.819883G>T GRCh37
NC_000011.8:g.809883G>T NCBI36
NG_023394.1:g.5983G>T

Transcript Alleles

HGVS Amino-acid Change
NM_020376.4:c.165G>T MANE Select NP_065109.1:p.Ala55=
ENST00000336615.9:c.165G>T MANE Select ENSP00000337701.4:p.Ala55=
NM_020376.3:c.165G>T NP_065109.1:p.Ala55=
ENST00000336615.8:c.165G>T ENSP00000337701.4:p.Ala55=
XM_006718265.2:c.165G>T XP_006718328.1:p.Ala55=
XM_006718265.3:c.165G>T XP_006718328.1:p.Ala55=
XM_006718266.2:c.165G>T XP_006718329.1:p.Ala55=
XM_006718266.3:c.165G>T XP_006718329.1:p.Ala55=
XM_017018028.1:c.165G>T XP_016873517.1:p.Ala55=
XM_024448618.1:c.165G>T XP_024304386.1:p.Ala55=