Canonical Allele Identifier: CA403138284

Gene: PNPLA6

Linked Data

• dbSNP Id: rs747377799
• gnomAD v3: 19-7561026-C-A
• gnomAD v4: 19-7561026-C-A
• MyVariant Identifiers: chr19:g.7625912C>A (hg19) ; chr19:g.7561026C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561026C>A , CM000681.2:g.7561026C>A	GRCh38
NC_000019.9:g.7625912C>A , CM000681.1:g.7625912C>A	GRCh37
NC_000019.8:g.7531912C>A	NCBI36
NG_013374.1:g.31875C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3829C>A MANE Select	ENSP00000473211.1:p.Pro1277Thr
ENST00000221249.10:c.3715C>A	ENSP00000221249.5:p.Pro1239Thr
ENST00000414982.7:c.3859C>A	ENSP00000407509.2:p.Pro1287Thr
ENST00000450331.7:c.3715C>A	ENSP00000394348.2:p.Pro1239Thr
ENST00000545201.6:c.3634C>A	ENSP00000443323.1:p.Pro1212Thr
ENST00000597202.1:n.187C>A
ENST00000599947.1:c.198C>A
ENST00000600737.5:c.3829C>A	ENSP00000473211.1:p.Pro1277Thr
NM_001166111.1:c.3859C>A	NP_001159583.1:p.Pro1287Thr
NM_001166112.1:c.3634C>A	NP_001159584.1:p.Pro1212Thr
NM_001166113.1:c.3715C>A	NP_001159585.1:p.Pro1239Thr
NM_001166114.1:c.3829C>A	NP_001159586.1:p.Pro1277Thr
NM_006702.4:c.3715C>A	NP_006693.3:p.Pro1239Thr
NM_001166111.2:c.3859C>A	NP_001159583.1:p.Pro1287Thr
NM_001166114.2:c.3829C>A MANE Select	NP_001159586.1:p.Pro1277Thr
NM_006702.5:c.3715C>A	NP_006693.3:p.Pro1239Thr
NM_001166112.2:c.3634C>A	NP_001159584.1:p.Pro1212Thr