Canonical Allele Identifier: CA2573880199
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.822312del , CM000673.2:g.822312del GRCh38
NC_000011.9:g.822312del , CM000673.1:g.822312del GRCh37
NC_000011.8:g.812312del NCBI36
NG_023394.1:g.8412del

Transcript Alleles

HGVS Amino-acid change
ENST00000336615.9:c.487-85del MANE Select ENSP00000337701.4:n.487-85del
ENST00000336615.8:c.487-85del ENSP00000337701.4:n.487-85del
ENST00000525250.5:n.1093-85del
ENST00000531923.1:n.297del
ENST00000617551.1:c.-764-85del ENSP00000481602.1:n.-764-85del
NM_020376.3:c.487-85del NP_065109.1:n.487-85del
XM_006718265.2:c.487-85del XP_006718328.1:n.487-85del
XM_006718266.2:c.487-85del XP_006718329.1:n.487-85del
XM_006718265.3:c.487-85del XP_006718328.1:n.487-85del
XM_006718266.3:c.487-85del XP_006718329.1:n.487-85del
XM_017018028.1:c.487-85del XP_016873517.1:n.487-85del
XM_024448618.1:c.487-85del XP_024304386.1:n.487-85del
NM_020376.4:c.487-85del MANE Select NP_065109.1:n.487-85del