Canonical Allele Identifier: CA2587958165
Gene: PNPLA6 HGNC NCBI

Linked Data

gnomAD v4: 19-7560620-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7560620C>A , CM000681.2:g.7560620C>A GRCh38
NC_000019.9:g.7625506C>A , CM000681.1:g.7625506C>A GRCh37
NC_000019.8:g.7531506C>A NCBI36
NG_013374.1:g.31469C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3700-28C>A MANE Select ENSP00000473211.1:n.3700-28C>A
ENST00000221249.10:c.3586-28C>A ENSP00000221249.5:n.3586-28C>A
ENST00000414982.7:c.3730-28C>A ENSP00000407509.2:n.3730-28C>A
ENST00000450331.7:c.3586-28C>A ENSP00000394348.2:n.3586-28C>A
ENST00000545201.6:c.3505-28C>A ENSP00000443323.1:n.3505-28C>A
ENST00000597202.1:n.30C>A
ENST00000599947.1:c.186-394C>A
ENST00000600737.5:c.3700-28C>A ENSP00000473211.1:n.3700-28C>A
NM_001166111.1:c.3730-28C>A NP_001159583.1:n.3730-28C>A
NM_001166112.1:c.3505-28C>A NP_001159584.1:n.3505-28C>A
NM_001166113.1:c.3586-28C>A NP_001159585.1:n.3586-28C>A
NM_001166114.1:c.3700-28C>A NP_001159586.1:n.3700-28C>A
NM_006702.4:c.3586-28C>A NP_006693.3:n.3586-28C>A
NM_001166111.2:c.3730-28C>A NP_001159583.1:n.3730-28C>A
NM_001166114.2:c.3700-28C>A MANE Select NP_001159586.1:n.3700-28C>A
NM_006702.5:c.3586-28C>A NP_006693.3:n.3586-28C>A
NM_001166112.2:c.3505-28C>A NP_001159584.1:n.3505-28C>A