Canonical Allele Identifier: CA216972144
Community Standard Title: NM_020376.4(PNPLA2):c.1266G>A (p.Trp422Ter)
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.824613G>A , CM000673.2:g.824613G>A GRCh38
NC_000011.9:g.824613G>A , CM000673.1:g.824613G>A GRCh37
NC_000011.8:g.814613G>A NCBI36
NG_023394.1:g.10713G>A

Transcript Alleles

HGVS Amino-acid Change
NM_020376.4:c.1266G>A MANE Select NP_065109.1:p.Trp422Ter
ENST00000336615.9:c.1266G>A MANE Select ENSP00000337701.4:p.Trp422Ter
NM_020376.3:c.1266G>A NP_065109.1:p.Trp422Ter
ENST00000336615.8:c.1266G>A ENSP00000337701.4:p.Trp422Ter
ENST00000525250.5:n.2120G>A
ENST00000529255.1:n.696G>A
ENST00000617551.1:c.264G>A ENSP00000481602.1:p.Trp88Ter
XM_006718265.2:c.1408G>A XP_006718328.1:p.Asp470Asn
XM_006718265.3:c.1408G>A XP_006718328.1:p.Asp470Asn
XM_006718266.2:c.1408G>A XP_006718329.1:p.Asp470Asn
XM_006718266.3:c.1408G>A XP_006718329.1:p.Asp470Asn
XM_017018028.1:c.1266G>A XP_016873517.1:p.Trp422Ter
XM_024448618.1:c.1494G>A XP_024304386.1:p.Trp498Ter