Canonical Allele Identifier: CA2813477602
Gene: PNPLA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7560898_7560899insAG , CM000681.2:g.7560898_7560899insAG GRCh38
NC_000019.9:g.7625784_7625785insAG , CM000681.1:g.7625784_7625785insAG GRCh37
NC_000019.8:g.7531784_7531785insAG NCBI36
NG_013374.1:g.31747_31748insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3817-116_3817-115insAG MANE Select ENSP00000473211.1:n.3817-116_3817-115insAG
ENST00000221249.10:c.3703-116_3703-115insAG ENSP00000221249.5:n.3703-116_3703-115insAG
ENST00000414982.7:c.3847-116_3847-115insAG ENSP00000407509.2:n.3847-116_3847-115insAG
ENST00000450331.7:c.3703-116_3703-115insAG ENSP00000394348.2:n.3703-116_3703-115insAG
ENST00000545201.6:c.3622-116_3622-115insAG ENSP00000443323.1:n.3622-116_3622-115insAG
ENST00000597202.1:n.175-116_175-115insAG
ENST00000599947.1:c.186-116_186-115insAG
ENST00000600737.5:c.3817-116_3817-115insAG ENSP00000473211.1:n.3817-116_3817-115insAG
NM_001166111.1:c.3847-116_3847-115insAG NP_001159583.1:n.3847-116_3847-115insAG
NM_001166112.1:c.3622-116_3622-115insAG NP_001159584.1:n.3622-116_3622-115insAG
NM_001166113.1:c.3703-116_3703-115insAG NP_001159585.1:n.3703-116_3703-115insAG
NM_001166114.1:c.3817-116_3817-115insAG NP_001159586.1:n.3817-116_3817-115insAG
NM_006702.4:c.3703-116_3703-115insAG NP_006693.3:n.3703-116_3703-115insAG
NM_001166111.2:c.3847-116_3847-115insAG NP_001159583.1:n.3847-116_3847-115insAG
NM_001166114.2:c.3817-116_3817-115insAG MANE Select NP_001159586.1:n.3817-116_3817-115insAG
NM_006702.5:c.3703-116_3703-115insAG NP_006693.3:n.3703-116_3703-115insAG
NM_001166112.2:c.3622-116_3622-115insAG NP_001159584.1:n.3622-116_3622-115insAG