Canonical Allele Identifier: CA403138517

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7625946T>C (hg19) ; chr19:g.7561060T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561060T>C , CM000681.2:g.7561060T>C	GRCh38
NC_000019.9:g.7625946T>C , CM000681.1:g.7625946T>C	GRCh37
NC_000019.8:g.7531946T>C	NCBI36
NG_013374.1:g.31909T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000600737.6:c.3863T>C MANE Select	ENSP00000473211.1:p.Val1288Ala
ENST00000221249.10:c.3749T>C	ENSP00000221249.5:p.Val1250Ala
ENST00000414982.7:c.3893T>C	ENSP00000407509.2:p.Val1298Ala
ENST00000450331.7:c.3749T>C	ENSP00000394348.2:p.Val1250Ala
ENST00000545201.6:c.3668T>C	ENSP00000443323.1:p.Val1223Ala
ENST00000597202.1:n.221T>C
ENST00000599947.1:c.232T>C
ENST00000600737.5:c.3863T>C	ENSP00000473211.1:p.Val1288Ala
NM_001166111.1:c.3893T>C	NP_001159583.1:p.Val1298Ala
NM_001166112.1:c.3668T>C	NP_001159584.1:p.Val1223Ala
NM_001166113.1:c.3749T>C	NP_001159585.1:p.Val1250Ala
NM_001166114.1:c.3863T>C	NP_001159586.1:p.Val1288Ala
NM_006702.4:c.3749T>C	NP_006693.3:p.Val1250Ala
NM_001166111.2:c.3893T>C	NP_001159583.1:p.Val1298Ala
NM_001166114.2:c.3863T>C MANE Select	NP_001159586.1:p.Val1288Ala
NM_006702.5:c.3749T>C	NP_006693.3:p.Val1250Ala
NM_001166112.2:c.3668T>C	NP_001159584.1:p.Val1223Ala