Canonical Allele Identifier: CA2320979338
Gene: PNPLA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7560713A= , CM000681.2:g.7560713A= GRCh38
NC_000019.9:g.7625599A= , CM000681.1:g.7625599A= GRCh37
NC_000019.8:g.7531599A= NCBI36
NG_013374.1:g.31562A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3765A= MANE Select ENSP00000473211.1:p.Lys1255=
ENST00000221249.10:c.3651A= ENSP00000221249.5:p.Lys1217=
ENST00000414982.7:c.3795A= ENSP00000407509.2:p.Lys1265=
ENST00000450331.7:c.3651A= ENSP00000394348.2:p.Lys1217=
ENST00000545201.6:c.3570A= ENSP00000443323.1:p.Lys1190=
ENST00000597202.1:n.123A=
ENST00000599947.1:c.186-301A=
ENST00000600737.5:c.3765A= ENSP00000473211.1:p.Lys1255=
NM_001166111.1:c.3795A= NP_001159583.1:p.Lys1265=
NM_001166112.1:c.3570A= NP_001159584.1:p.Lys1190=
NM_001166113.1:c.3651A= NP_001159585.1:p.Lys1217=
NM_001166114.1:c.3765A= NP_001159586.1:p.Lys1255=
NM_006702.4:c.3651A= NP_006693.3:p.Lys1217=
NM_001166111.2:c.3795A= NP_001159583.1:p.Lys1265=
NM_001166114.2:c.3765A= MANE Select NP_001159586.1:p.Lys1255=
NM_006702.5:c.3651A= NP_006693.3:p.Lys1217=
NM_001166112.2:c.3570A= NP_001159584.1:p.Lys1190=