Canonical Allele Identifier: CA2320979513
Gene: PNPLA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7561030G= , CM000681.2:g.7561030G= GRCh38
NC_000019.9:g.7625916G= , CM000681.1:g.7625916G= GRCh37
NC_000019.8:g.7531916G= NCBI36
NG_013374.1:g.31879G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3833G= MANE Select ENSP00000473211.1:p.Ser1278=
ENST00000221249.10:c.3719G= ENSP00000221249.5:p.Ser1240=
ENST00000414982.7:c.3863G= ENSP00000407509.2:p.Ser1288=
ENST00000450331.7:c.3719G= ENSP00000394348.2:p.Ser1240=
ENST00000545201.6:c.3638G= ENSP00000443323.1:p.Ser1213=
ENST00000597202.1:n.191G=
ENST00000599947.1:c.202G=
ENST00000600737.5:c.3833G= ENSP00000473211.1:p.Ser1278=
NM_001166111.1:c.3863G= NP_001159583.1:p.Ser1288=
NM_001166112.1:c.3638G= NP_001159584.1:p.Ser1213=
NM_001166113.1:c.3719G= NP_001159585.1:p.Ser1240=
NM_001166114.1:c.3833G= NP_001159586.1:p.Ser1278=
NM_006702.4:c.3719G= NP_006693.3:p.Ser1240=
NM_001166111.2:c.3863G= NP_001159583.1:p.Ser1288=
NM_001166114.2:c.3833G= MANE Select NP_001159586.1:p.Ser1278=
NM_006702.5:c.3719G= NP_006693.3:p.Ser1240=
NM_001166112.2:c.3638G= NP_001159584.1:p.Ser1213=