Canonical Allele Identifier: CA403137985

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7625646C>G (hg19) ; chr19:g.7560760C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560760C>G , CM000681.2:g.7560760C>G	GRCh38
NC_000019.9:g.7625646C>G , CM000681.1:g.7625646C>G	GRCh37
NC_000019.8:g.7531646C>G	NCBI36
NG_013374.1:g.31609C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3812C>G MANE Select	ENSP00000473211.1:p.Ala1271Gly
ENST00000221249.10:c.3698C>G	ENSP00000221249.5:p.Ala1233Gly
ENST00000414982.7:c.3842C>G	ENSP00000407509.2:p.Ala1281Gly
ENST00000450331.7:c.3698C>G	ENSP00000394348.2:p.Ala1233Gly
ENST00000545201.6:c.3617C>G	ENSP00000443323.1:p.Ala1206Gly
ENST00000597202.1:n.170C>G
ENST00000599947.1:c.186-254C>G
ENST00000600737.5:c.3812C>G	ENSP00000473211.1:p.Ala1271Gly
NM_001166111.1:c.3842C>G	NP_001159583.1:p.Ala1281Gly
NM_001166112.1:c.3617C>G	NP_001159584.1:p.Ala1206Gly
NM_001166113.1:c.3698C>G	NP_001159585.1:p.Ala1233Gly
NM_001166114.1:c.3812C>G	NP_001159586.1:p.Ala1271Gly
NM_006702.4:c.3698C>G	NP_006693.3:p.Ala1233Gly
NM_001166111.2:c.3842C>G	NP_001159583.1:p.Ala1281Gly
NM_001166114.2:c.3812C>G MANE Select	NP_001159586.1:p.Ala1271Gly
NM_006702.5:c.3698C>G	NP_006693.3:p.Ala1233Gly
NM_001166112.2:c.3617C>G	NP_001159584.1:p.Ala1206Gly