Canonical Allele Identifier: CA9140658

Gene: PNPLA6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561284C>T , CM000681.2:g.7561284C>T	GRCh38
NC_000019.9:g.7626170C>T , CM000681.1:g.7626170C>T	GRCh37
NC_000019.8:g.7532170C>T	NCBI36
NG_013374.1:g.32133C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001166114.2:c.3990C>T MANE Select	NP_001159586.1:p.Pro1330=
ENST00000600737.6:c.3990C>T MANE Select	ENSP00000473211.1:p.Pro1330=
NM_001166111.1:c.4020C>T	NP_001159583.1:p.Pro1340=
NM_001166111.2:c.4020C>T	NP_001159583.1:p.Pro1340=
NM_001166112.1:c.3795C>T	NP_001159584.1:p.Pro1265=
NM_001166112.2:c.3795C>T	NP_001159584.1:p.Pro1265=
NM_001166113.1:c.3876C>T	NP_001159585.1:p.Pro1292=
NM_001166114.1:c.3990C>T	NP_001159586.1:p.Pro1330=
NM_006702.4:c.3876C>T	NP_006693.3:p.Pro1292=
NM_006702.5:c.3876C>T	NP_006693.3:p.Pro1292=
ENST00000221249.10:c.3876C>T	ENSP00000221249.5:p.Pro1292=
ENST00000414982.7:c.4020C>T	ENSP00000407509.2:p.Pro1340=
ENST00000450331.7:c.3876C>T	ENSP00000394348.2:p.Pro1292=
ENST00000545201.6:c.3795C>T	ENSP00000443323.1:p.Pro1265=
ENST00000597202.1:n.348C>T
ENST00000599947.1:c.359C>T
ENST00000600737.5:c.3990C>T	ENSP00000473211.1:p.Pro1330=