Canonical Allele Identifier: CA403134838

Gene: PNPLA6

Linked Data

• ClinVar Variation Id: 469619
• ClinVar RCV Id: RCV000539525
• dbSNP Id: rs1555751597
• MyVariant Identifiers: chr19:g.7623841G>A (hg19) ; chr19:g.7558955G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7558955G>A , CM000681.2:g.7558955G>A	GRCh38
NC_000019.9:g.7623841G>A , CM000681.1:g.7623841G>A	GRCh37
NC_000019.8:g.7529841G>A	NCBI36
NG_013374.1:g.29804G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3503G>A MANE Select	ENSP00000473211.1:p.Trp1168Ter
ENST00000221249.10:c.3389G>A	ENSP00000221249.5:p.Trp1130Ter
ENST00000414982.7:c.3533G>A	ENSP00000407509.2:p.Trp1178Ter
ENST00000450331.7:c.3389G>A	ENSP00000394348.2:p.Trp1130Ter
ENST00000545201.6:c.3308G>A	ENSP00000443323.1:p.Trp1103Ter
ENST00000600737.5:c.3503G>A	ENSP00000473211.1:p.Trp1168Ter
NM_001166111.1:c.3533G>A	NP_001159583.1:p.Trp1178Ter
NM_001166112.1:c.3308G>A	NP_001159584.1:p.Trp1103Ter
NM_001166113.1:c.3389G>A	NP_001159585.1:p.Trp1130Ter
NM_001166114.1:c.3503G>A	NP_001159586.1:p.Trp1168Ter
NM_006702.4:c.3389G>A	NP_006693.3:p.Trp1130Ter
NM_001166111.2:c.3533G>A	NP_001159583.1:p.Trp1178Ter
NM_001166114.2:c.3503G>A MANE Select	NP_001159586.1:p.Trp1168Ter
NM_006702.5:c.3389G>A	NP_006693.3:p.Trp1130Ter
NM_001166112.2:c.3308G>A	NP_001159584.1:p.Trp1103Ter