Canonical Allele Identifier: CA403138190

Gene: PNPLA6

Linked Data

• ClinVar Variation Id: 892672
• ClinVar RCV Id: RCV001129028
• dbSNP Id: rs1164847477
• gnomAD v2: 19-7625900-G-A
• gnomAD v4: 19-7561014-G-A
• MyVariant Identifiers: chr19:g.7625900G>A (hg19) ; chr19:g.7561014G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561014G>A , CM000681.2:g.7561014G>A	GRCh38
NC_000019.9:g.7625900G>A , CM000681.1:g.7625900G>A	GRCh37
NC_000019.8:g.7531900G>A	NCBI36
NG_013374.1:g.31863G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3817G>A MANE Select	ENSP00000473211.1:p.Val1273Met
ENST00000221249.10:c.3703G>A	ENSP00000221249.5:p.Val1235Met
ENST00000414982.7:c.3847G>A	ENSP00000407509.2:p.Val1283Met
ENST00000450331.7:c.3703G>A	ENSP00000394348.2:p.Val1235Met
ENST00000545201.6:c.3622G>A	ENSP00000443323.1:p.Val1208Met
ENST00000597202.1:n.175G>A
ENST00000599947.1:c.186G>A
ENST00000600737.5:c.3817G>A	ENSP00000473211.1:p.Val1273Met
NM_001166111.1:c.3847G>A	NP_001159583.1:p.Val1283Met
NM_001166112.1:c.3622G>A	NP_001159584.1:p.Val1208Met
NM_001166113.1:c.3703G>A	NP_001159585.1:p.Val1235Met
NM_001166114.1:c.3817G>A	NP_001159586.1:p.Val1273Met
NM_006702.4:c.3703G>A	NP_006693.3:p.Val1235Met
NM_001166111.2:c.3847G>A	NP_001159583.1:p.Val1283Met
NM_001166114.2:c.3817G>A MANE Select	NP_001159586.1:p.Val1273Met
NM_006702.5:c.3703G>A	NP_006693.3:p.Val1235Met
NM_001166112.2:c.3622G>A	NP_001159584.1:p.Val1208Met