Canonical Allele Identifier: CA403138758

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7625982A>C (hg19) ; chr19:g.7561096A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561096A>C , CM000681.2:g.7561096A>C	GRCh38
NC_000019.9:g.7625982A>C , CM000681.1:g.7625982A>C	GRCh37
NC_000019.8:g.7531982A>C	NCBI36
NG_013374.1:g.31945A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3899A>C MANE Select	ENSP00000473211.1:p.Asp1300Ala
ENST00000221249.10:c.3785A>C	ENSP00000221249.5:p.Asp1262Ala
ENST00000414982.7:c.3929A>C	ENSP00000407509.2:p.Asp1310Ala
ENST00000450331.7:c.3785A>C	ENSP00000394348.2:p.Asp1262Ala
ENST00000545201.6:c.3704A>C	ENSP00000443323.1:p.Asp1235Ala
ENST00000597202.1:n.257A>C
ENST00000599947.1:c.268A>C
ENST00000600737.5:c.3899A>C	ENSP00000473211.1:p.Asp1300Ala
NM_001166111.1:c.3929A>C	NP_001159583.1:p.Asp1310Ala
NM_001166112.1:c.3704A>C	NP_001159584.1:p.Asp1235Ala
NM_001166113.1:c.3785A>C	NP_001159585.1:p.Asp1262Ala
NM_001166114.1:c.3899A>C	NP_001159586.1:p.Asp1300Ala
NM_006702.4:c.3785A>C	NP_006693.3:p.Asp1262Ala
NM_001166111.2:c.3929A>C	NP_001159583.1:p.Asp1310Ala
NM_001166114.2:c.3899A>C MANE Select	NP_001159586.1:p.Asp1300Ala
NM_006702.5:c.3785A>C	NP_006693.3:p.Asp1262Ala
NM_001166112.2:c.3704A>C	NP_001159584.1:p.Asp1235Ala