Canonical Allele Identifier: CA403133695

Gene: PNPLA6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7557179C>T , CM000681.2:g.7557179C>T	GRCh38
NC_000019.9:g.7622065C>T , CM000681.1:g.7622065C>T	GRCh37
NC_000019.8:g.7528065C>T	NCBI36
NG_013374.1:g.28028C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001166114.2:c.3292C>T MANE Select	NP_001159586.1:p.Arg1098Trp
ENST00000600737.6:c.3292C>T MANE Select	ENSP00000473211.1:p.Arg1098Trp
NM_001166111.1:c.3322C>T	NP_001159583.1:p.Arg1108Trp
NM_001166111.2:c.3322C>T	NP_001159583.1:p.Arg1108Trp
NM_001166112.1:c.3097C>T	NP_001159584.1:p.Arg1033Trp
NM_001166112.2:c.3097C>T	NP_001159584.1:p.Arg1033Trp
NM_001166113.1:c.3178C>T	NP_001159585.1:p.Arg1060Trp
NM_001166114.1:c.3292C>T	NP_001159586.1:p.Arg1098Trp
NM_006702.4:c.3178C>T	NP_006693.3:p.Arg1060Trp
NM_006702.5:c.3178C>T	NP_006693.3:p.Arg1060Trp
ENST00000221249.10:c.3178C>T	ENSP00000221249.5:p.Arg1060Trp
ENST00000414982.7:c.3322C>T	ENSP00000407509.2:p.Arg1108Trp
ENST00000450331.7:c.3178C>T	ENSP00000394348.2:p.Arg1060Trp
ENST00000545201.6:c.3097C>T	ENSP00000443323.1:p.Arg1033Trp
ENST00000595352.1:n.223C>T
ENST00000600737.5:c.3292C>T	ENSP00000473211.1:p.Arg1098Trp
ENST00000646984.1:c.568+97C>T	ENSP00000496219.1:n.568+97C>T