Canonical Allele Identifier: CA2320979582
Gene: PNPLA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7561170C= , CM000681.2:g.7561170C= GRCh38
NC_000019.9:g.7626056C= , CM000681.1:g.7626056C= GRCh37
NC_000019.8:g.7532056C= NCBI36
NG_013374.1:g.32019C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3914-38C= MANE Select ENSP00000473211.1:n.3914-38C=
ENST00000221249.10:c.3800-38C= ENSP00000221249.5:n.3800-38C=
ENST00000414982.7:c.3944-38C= ENSP00000407509.2:n.3944-38C=
ENST00000450331.7:c.3800-38C= ENSP00000394348.2:n.3800-38C=
ENST00000545201.6:c.3719-38C= ENSP00000443323.1:n.3719-38C=
ENST00000597202.1:n.272-38C=
ENST00000599947.1:c.283-38C=
ENST00000600737.5:c.3914-38C= ENSP00000473211.1:n.3914-38C=
NM_001166111.1:c.3944-38C= NP_001159583.1:n.3944-38C=
NM_001166112.1:c.3719-38C= NP_001159584.1:n.3719-38C=
NM_001166113.1:c.3800-38C= NP_001159585.1:n.3800-38C=
NM_001166114.1:c.3914-38C= NP_001159586.1:n.3914-38C=
NM_006702.4:c.3800-38C= NP_006693.3:n.3800-38C=
NM_001166111.2:c.3944-38C= NP_001159583.1:n.3944-38C=
NM_001166114.2:c.3914-38C= MANE Select NP_001159586.1:n.3914-38C=
NM_006702.5:c.3800-38C= NP_006693.3:n.3800-38C=
NM_001166112.2:c.3719-38C= NP_001159584.1:n.3719-38C=