Canonical Allele Identifier: CA2576598126
Gene: PNPLA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7560956dup , CM000681.2:g.7560956dup GRCh38
NC_000019.9:g.7625842dup , CM000681.1:g.7625842dup GRCh37
NC_000019.8:g.7531842dup NCBI36
NG_013374.1:g.31805dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3817-58dup MANE Select ENSP00000473211.1:n.3817-58dup
ENST00000221249.10:c.3703-58dup ENSP00000221249.5:n.3703-58dup
ENST00000414982.7:c.3847-58dup ENSP00000407509.2:n.3847-58dup
ENST00000450331.7:c.3703-58dup ENSP00000394348.2:n.3703-58dup
ENST00000545201.6:c.3622-58dup ENSP00000443323.1:n.3622-58dup
ENST00000597202.1:n.175-58dup
ENST00000599947.1:c.186-58dup
ENST00000600737.5:c.3817-58dup ENSP00000473211.1:n.3817-58dup
NM_001166111.1:c.3847-58dup NP_001159583.1:n.3847-58dup
NM_001166112.1:c.3622-58dup NP_001159584.1:n.3622-58dup
NM_001166113.1:c.3703-58dup NP_001159585.1:n.3703-58dup
NM_001166114.1:c.3817-58dup NP_001159586.1:n.3817-58dup
NM_006702.4:c.3703-58dup NP_006693.3:n.3703-58dup
NM_001166111.2:c.3847-58dup NP_001159583.1:n.3847-58dup
NM_001166114.2:c.3817-58dup MANE Select NP_001159586.1:n.3817-58dup
NM_006702.5:c.3703-58dup NP_006693.3:n.3703-58dup
NM_001166112.2:c.3622-58dup NP_001159584.1:n.3622-58dup