Canonical Allele Identifier: CA505245167

Gene: PNPLA6

Linked Data

• gnomAD v4: 19-7560704-C-T
• MyVariant Identifiers: chr19:g.7625590C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560704C>T , CM000681.2:g.7560704C>T	GRCh38
NC_000019.9:g.7625590C>T , CM000681.1:g.7625590C>T	GRCh37
NC_000019.8:g.7531590C>T	NCBI36
NG_013374.1:g.31553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3756C>T MANE Select	ENSP00000473211.1:p.Val1252=
ENST00000221249.10:c.3642C>T	ENSP00000221249.5:p.Val1214=
ENST00000414982.7:c.3786C>T	ENSP00000407509.2:p.Val1262=
ENST00000450331.7:c.3642C>T	ENSP00000394348.2:p.Val1214=
ENST00000545201.6:c.3561C>T	ENSP00000443323.1:p.Val1187=
ENST00000597202.1:n.114C>T
ENST00000599947.1:c.186-310C>T
ENST00000600737.5:c.3756C>T	ENSP00000473211.1:p.Val1252=
NM_001166111.1:c.3786C>T	NP_001159583.1:p.Val1262=
NM_001166112.1:c.3561C>T	NP_001159584.1:p.Val1187=
NM_001166113.1:c.3642C>T	NP_001159585.1:p.Val1214=
NM_001166114.1:c.3756C>T	NP_001159586.1:p.Val1252=
NM_006702.4:c.3642C>T	NP_006693.3:p.Val1214=
NM_001166111.2:c.3786C>T	NP_001159583.1:p.Val1262=
NM_001166114.2:c.3756C>T MANE Select	NP_001159586.1:p.Val1252=
NM_006702.5:c.3642C>T	NP_006693.3:p.Val1214=
NM_001166112.2:c.3561C>T	NP_001159584.1:p.Val1187=