Canonical Allele Identifier: CA403137581

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7625579C>G (hg19) ; chr19:g.7560693C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560693C>G , CM000681.2:g.7560693C>G	GRCh38
NC_000019.9:g.7625579C>G , CM000681.1:g.7625579C>G	GRCh37
NC_000019.8:g.7531579C>G	NCBI36
NG_013374.1:g.31542C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3745C>G MANE Select	ENSP00000473211.1:p.Arg1249Gly
ENST00000221249.10:c.3631C>G	ENSP00000221249.5:p.Arg1211Gly
ENST00000414982.7:c.3775C>G	ENSP00000407509.2:p.Arg1259Gly
ENST00000450331.7:c.3631C>G	ENSP00000394348.2:p.Arg1211Gly
ENST00000545201.6:c.3550C>G	ENSP00000443323.1:p.Arg1184Gly
ENST00000597202.1:n.103C>G
ENST00000599947.1:c.186-321C>G
ENST00000600737.5:c.3745C>G	ENSP00000473211.1:p.Arg1249Gly
NM_001166111.1:c.3775C>G	NP_001159583.1:p.Arg1259Gly
NM_001166112.1:c.3550C>G	NP_001159584.1:p.Arg1184Gly
NM_001166113.1:c.3631C>G	NP_001159585.1:p.Arg1211Gly
NM_001166114.1:c.3745C>G	NP_001159586.1:p.Arg1249Gly
NM_006702.4:c.3631C>G	NP_006693.3:p.Arg1211Gly
NM_001166111.2:c.3775C>G	NP_001159583.1:p.Arg1259Gly
NM_001166114.2:c.3745C>G MANE Select	NP_001159586.1:p.Arg1249Gly
NM_006702.5:c.3631C>G	NP_006693.3:p.Arg1211Gly
NM_001166112.2:c.3550C>G	NP_001159584.1:p.Arg1184Gly