Canonical Allele Identifier: CA2320979314

Gene: PNPLA6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560660C= , CM000681.2:g.7560660C=	GRCh38
NC_000019.9:g.7625546C= , CM000681.1:g.7625546C=	GRCh37
NC_000019.8:g.7531546C=	NCBI36
NG_013374.1:g.31509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3712C= MANE Select	ENSP00000473211.1:p.Gln1238=
ENST00000221249.10:c.3598C=	ENSP00000221249.5:p.Gln1200=
ENST00000414982.7:c.3742C=	ENSP00000407509.2:p.Gln1248=
ENST00000450331.7:c.3598C=	ENSP00000394348.2:p.Gln1200=
ENST00000545201.6:c.3517C=	ENSP00000443323.1:p.Gln1173=
ENST00000597202.1:n.70C=
ENST00000599947.1:c.186-354C=
ENST00000600737.5:c.3712C=	ENSP00000473211.1:p.Gln1238=
NM_001166111.1:c.3742C=	NP_001159583.1:p.Gln1248=
NM_001166112.1:c.3517C=	NP_001159584.1:p.Gln1173=
NM_001166113.1:c.3598C=	NP_001159585.1:p.Gln1200=
NM_001166114.1:c.3712C=	NP_001159586.1:p.Gln1238=
NM_006702.4:c.3598C=	NP_006693.3:p.Gln1200=
NM_001166111.2:c.3742C=	NP_001159583.1:p.Gln1248=
NM_001166114.2:c.3712C= MANE Select	NP_001159586.1:p.Gln1238=
NM_006702.5:c.3598C=	NP_006693.3:p.Gln1200=
NM_001166112.2:c.3517C=	NP_001159584.1:p.Gln1173=