Canonical Allele Identifier: CA378978640
Gene: PNPLA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.821856T>G , CM000673.2:g.821856T>G GRCh38
NC_000011.9:g.821856T>G , CM000673.1:g.821856T>G GRCh37
NC_000011.8:g.811856T>G NCBI36
NG_023394.1:g.7956T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336615.9:c.416T>G MANE Select ENSP00000337701.4:p.Ile139Ser
ENST00000336615.8:c.416T>G ENSP00000337701.4:p.Ile139Ser
ENST00000525250.5:n.1022T>G
ENST00000534561.1:n.83T>G
ENST00000617551.1:c.-835T>G ENSP00000481602.1:n.-835T>G
NM_020376.3:c.416T>G NP_065109.1:p.Ile139Ser
XM_006718265.2:c.416T>G XP_006718328.1:p.Ile139Ser
XM_006718266.2:c.416T>G XP_006718329.1:p.Ile139Ser
XM_006718265.3:c.416T>G XP_006718328.1:p.Ile139Ser
XM_006718266.3:c.416T>G XP_006718329.1:p.Ile139Ser
XM_017018028.1:c.416T>G XP_016873517.1:p.Ile139Ser
XM_024448618.1:c.416T>G XP_024304386.1:p.Ile139Ser
NM_020376.4:c.416T>G MANE Select NP_065109.1:p.Ile139Ser