Canonical Allele Identifier: CA2581368037
Gene: PNPLA6 HGNC NCBI

Linked Data

gnomAD v4: 19-7560988-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7560988A>C , CM000681.2:g.7560988A>C GRCh38
NC_000019.9:g.7625874A>C , CM000681.1:g.7625874A>C GRCh37
NC_000019.8:g.7531874A>C NCBI36
NG_013374.1:g.31837A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3817-26A>C MANE Select ENSP00000473211.1:n.3817-26A>C
ENST00000221249.10:c.3703-26A>C ENSP00000221249.5:n.3703-26A>C
ENST00000414982.7:c.3847-26A>C ENSP00000407509.2:n.3847-26A>C
ENST00000450331.7:c.3703-26A>C ENSP00000394348.2:n.3703-26A>C
ENST00000545201.6:c.3622-26A>C ENSP00000443323.1:n.3622-26A>C
ENST00000597202.1:n.175-26A>C
ENST00000599947.1:c.186-26A>C
ENST00000600737.5:c.3817-26A>C ENSP00000473211.1:n.3817-26A>C
NM_001166111.1:c.3847-26A>C NP_001159583.1:n.3847-26A>C
NM_001166112.1:c.3622-26A>C NP_001159584.1:n.3622-26A>C
NM_001166113.1:c.3703-26A>C NP_001159585.1:n.3703-26A>C
NM_001166114.1:c.3817-26A>C NP_001159586.1:n.3817-26A>C
NM_006702.4:c.3703-26A>C NP_006693.3:n.3703-26A>C
NM_001166111.2:c.3847-26A>C NP_001159583.1:n.3847-26A>C
NM_001166114.2:c.3817-26A>C MANE Select NP_001159586.1:n.3817-26A>C
NM_006702.5:c.3703-26A>C NP_006693.3:n.3703-26A>C
NM_001166112.2:c.3622-26A>C NP_001159584.1:n.3622-26A>C