Canonical Allele Identifier: CA5791303
Community Standard Title: NM_020376.4(PNPLA2):c.1090C>T (p.Arg364Trp)
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.824351C>T , CM000673.2:g.824351C>T GRCh38
NC_000011.9:g.824351C>T , CM000673.1:g.824351C>T GRCh37
NC_000011.8:g.814351C>T NCBI36
NG_023394.1:g.10451C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020376.4:c.1090C>T MANE Select NP_065109.1:p.Arg364Trp
ENST00000336615.9:c.1090C>T MANE Select ENSP00000337701.4:p.Arg364Trp
NM_020376.3:c.1090C>T NP_065109.1:p.Arg364Trp
ENST00000336615.8:c.1090C>T ENSP00000337701.4:p.Arg364Trp
ENST00000525250.5:n.1944C>T
ENST00000526083.1:n.379C>T
ENST00000529255.1:n.520C>T
ENST00000617551.1:c.88C>T ENSP00000481602.1:p.Arg30Trp
XM_006718265.2:c.1232C>T XP_006718328.1:p.Pro411Leu
XM_006718265.3:c.1232C>T XP_006718328.1:p.Pro411Leu
XM_006718266.2:c.1232C>T XP_006718329.1:p.Pro411Leu
XM_006718266.3:c.1232C>T XP_006718329.1:p.Pro411Leu
XM_017018028.1:c.1090C>T XP_016873517.1:p.Arg364Trp
XM_024448618.1:c.1232C>T XP_024304386.1:p.Pro411Leu