Canonical Allele Identifier: CA505245105

Gene: PNPLA6

Linked Data

• ClinVar Variation Id: 2758765
• ClinVar RCV Id: RCV003507176
• MyVariant Identifiers: chr19:g.7625545C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560659C>T , CM000681.2:g.7560659C>T	GRCh38
NC_000019.9:g.7625545C>T , CM000681.1:g.7625545C>T	GRCh37
NC_000019.8:g.7531545C>T	NCBI36
NG_013374.1:g.31508C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3711C>T MANE Select	ENSP00000473211.1:p.Tyr1237=
ENST00000221249.10:c.3597C>T	ENSP00000221249.5:p.Tyr1199=
ENST00000414982.7:c.3741C>T	ENSP00000407509.2:p.Tyr1247=
ENST00000450331.7:c.3597C>T	ENSP00000394348.2:p.Tyr1199=
ENST00000545201.6:c.3516C>T	ENSP00000443323.1:p.Tyr1172=
ENST00000597202.1:n.69C>T
ENST00000599947.1:c.186-355C>T
ENST00000600737.5:c.3711C>T	ENSP00000473211.1:p.Tyr1237=
NM_001166111.1:c.3741C>T	NP_001159583.1:p.Tyr1247=
NM_001166112.1:c.3516C>T	NP_001159584.1:p.Tyr1172=
NM_001166113.1:c.3597C>T	NP_001159585.1:p.Tyr1199=
NM_001166114.1:c.3711C>T	NP_001159586.1:p.Tyr1237=
NM_006702.4:c.3597C>T	NP_006693.3:p.Tyr1199=
NM_001166111.2:c.3741C>T	NP_001159583.1:p.Tyr1247=
NM_001166114.2:c.3711C>T MANE Select	NP_001159586.1:p.Tyr1237=
NM_006702.5:c.3597C>T	NP_006693.3:p.Tyr1199=
NM_001166112.2:c.3516C>T	NP_001159584.1:p.Tyr1172=