Canonical Allele Identifier: CA505404361

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7625992T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561106T>G , CM000681.2:g.7561106T>G	GRCh38
NC_000019.9:g.7625992T>G , CM000681.1:g.7625992T>G	GRCh37
NC_000019.8:g.7531992T>G	NCBI36
NG_013374.1:g.31955T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3909T>G MANE Select	ENSP00000473211.1:p.Ala1303=
ENST00000221249.10:c.3795T>G	ENSP00000221249.5:p.Ala1265=
ENST00000414982.7:c.3939T>G	ENSP00000407509.2:p.Ala1313=
ENST00000450331.7:c.3795T>G	ENSP00000394348.2:p.Ala1265=
ENST00000545201.6:c.3714T>G	ENSP00000443323.1:p.Ala1238=
ENST00000597202.1:n.267T>G
ENST00000599947.1:c.278T>G
ENST00000600737.5:c.3909T>G	ENSP00000473211.1:p.Ala1303=
NM_001166111.1:c.3939T>G	NP_001159583.1:p.Ala1313=
NM_001166112.1:c.3714T>G	NP_001159584.1:p.Ala1238=
NM_001166113.1:c.3795T>G	NP_001159585.1:p.Ala1265=
NM_001166114.1:c.3909T>G	NP_001159586.1:p.Ala1303=
NM_006702.4:c.3795T>G	NP_006693.3:p.Ala1265=
NM_001166111.2:c.3939T>G	NP_001159583.1:p.Ala1313=
NM_001166114.2:c.3909T>G MANE Select	NP_001159586.1:p.Ala1303=
NM_006702.5:c.3795T>G	NP_006693.3:p.Ala1265=
NM_001166112.2:c.3714T>G	NP_001159584.1:p.Ala1238=