Canonical Allele Identifier: CA403137602

Gene: PNPLA6

Linked Data

• gnomAD v4: 19-7560697-G-A
• MyVariant Identifiers: chr19:g.7625583G>A (hg19) ; chr19:g.7560697G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560697G>A , CM000681.2:g.7560697G>A	GRCh38
NC_000019.9:g.7625583G>A , CM000681.1:g.7625583G>A	GRCh37
NC_000019.8:g.7531583G>A	NCBI36
NG_013374.1:g.31546G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3749G>A MANE Select	ENSP00000473211.1:p.Gly1250Asp
ENST00000221249.10:c.3635G>A	ENSP00000221249.5:p.Gly1212Asp
ENST00000414982.7:c.3779G>A	ENSP00000407509.2:p.Gly1260Asp
ENST00000450331.7:c.3635G>A	ENSP00000394348.2:p.Gly1212Asp
ENST00000545201.6:c.3554G>A	ENSP00000443323.1:p.Gly1185Asp
ENST00000597202.1:n.107G>A
ENST00000599947.1:c.186-317G>A
ENST00000600737.5:c.3749G>A	ENSP00000473211.1:p.Gly1250Asp
NM_001166111.1:c.3779G>A	NP_001159583.1:p.Gly1260Asp
NM_001166112.1:c.3554G>A	NP_001159584.1:p.Gly1185Asp
NM_001166113.1:c.3635G>A	NP_001159585.1:p.Gly1212Asp
NM_001166114.1:c.3749G>A	NP_001159586.1:p.Gly1250Asp
NM_006702.4:c.3635G>A	NP_006693.3:p.Gly1212Asp
NM_001166111.2:c.3779G>A	NP_001159583.1:p.Gly1260Asp
NM_001166114.2:c.3749G>A MANE Select	NP_001159586.1:p.Gly1250Asp
NM_006702.5:c.3635G>A	NP_006693.3:p.Gly1212Asp
NM_001166112.2:c.3554G>A	NP_001159584.1:p.Gly1185Asp