Canonical Allele Identifier: CA2320979352

Gene: PNPLA6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560739A= , CM000681.2:g.7560739A=	GRCh38
NC_000019.9:g.7625625A= , CM000681.1:g.7625625A=	GRCh37
NC_000019.8:g.7531625A=	NCBI36
NG_013374.1:g.31588A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3791A= MANE Select	ENSP00000473211.1:p.Asp1264=
ENST00000221249.10:c.3677A=	ENSP00000221249.5:p.Asp1226=
ENST00000414982.7:c.3821A=	ENSP00000407509.2:p.Asp1274=
ENST00000450331.7:c.3677A=	ENSP00000394348.2:p.Asp1226=
ENST00000545201.6:c.3596A=	ENSP00000443323.1:p.Asp1199=
ENST00000597202.1:n.149A=
ENST00000599947.1:c.186-275A=
ENST00000600737.5:c.3791A=	ENSP00000473211.1:p.Asp1264=
NM_001166111.1:c.3821A=	NP_001159583.1:p.Asp1274=
NM_001166112.1:c.3596A=	NP_001159584.1:p.Asp1199=
NM_001166113.1:c.3677A=	NP_001159585.1:p.Asp1226=
NM_001166114.1:c.3791A=	NP_001159586.1:p.Asp1264=
NM_006702.4:c.3677A=	NP_006693.3:p.Asp1226=
NM_001166111.2:c.3821A=	NP_001159583.1:p.Asp1274=
NM_001166114.2:c.3791A= MANE Select	NP_001159586.1:p.Asp1264=
NM_006702.5:c.3677A=	NP_006693.3:p.Asp1226=
NM_001166112.2:c.3596A=	NP_001159584.1:p.Asp1199=