Canonical Allele Identifier: CA403139107

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7626115C>G (hg19) ; chr19:g.7561229C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561229C>G , CM000681.2:g.7561229C>G	GRCh38
NC_000019.9:g.7626115C>G , CM000681.1:g.7626115C>G	GRCh37
NC_000019.8:g.7532115C>G	NCBI36
NG_013374.1:g.32078C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3935C>G MANE Select	ENSP00000473211.1:p.Thr1312Arg
ENST00000221249.10:c.3821C>G	ENSP00000221249.5:p.Thr1274Arg
ENST00000414982.7:c.3965C>G	ENSP00000407509.2:p.Thr1322Arg
ENST00000450331.7:c.3821C>G	ENSP00000394348.2:p.Thr1274Arg
ENST00000545201.6:c.3740C>G	ENSP00000443323.1:p.Thr1247Arg
ENST00000597202.1:n.293C>G
ENST00000599947.1:c.304C>G
ENST00000600737.5:c.3935C>G	ENSP00000473211.1:p.Thr1312Arg
NM_001166111.1:c.3965C>G	NP_001159583.1:p.Thr1322Arg
NM_001166112.1:c.3740C>G	NP_001159584.1:p.Thr1247Arg
NM_001166113.1:c.3821C>G	NP_001159585.1:p.Thr1274Arg
NM_001166114.1:c.3935C>G	NP_001159586.1:p.Thr1312Arg
NM_006702.4:c.3821C>G	NP_006693.3:p.Thr1274Arg
NM_001166111.2:c.3965C>G	NP_001159583.1:p.Thr1322Arg
NM_001166114.2:c.3935C>G MANE Select	NP_001159586.1:p.Thr1312Arg
NM_006702.5:c.3821C>G	NP_006693.3:p.Thr1274Arg
NM_001166112.2:c.3740C>G	NP_001159584.1:p.Thr1247Arg