Canonical Allele Identifier: CA631463029
Gene: PNPLA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7535831dup , CM000681.2:g.7535831dup GRCh38
NC_000019.9:g.7600717dup , CM000681.1:g.7600717dup GRCh37
NC_000019.8:g.7506717dup NCBI36
NG_013374.1:g.6680dup
NG_015806.1:g.18222dup

Transcript Alleles

HGVS Amino-acid Change
NM_001166114.2:c.43dup MANE Select NP_001159586.1:p.Ala15GlyfsTer?
ENST00000600737.6:c.43dup MANE Select ENSP00000473211.1:p.Ala15GlyfsTer?
NM_001166111.1:c.70dup NP_001159583.1:p.Ala24GlyfsTer?
NM_001166111.2:c.70dup NP_001159583.1:p.Ala24GlyfsTer?
NM_001166112.1:c.28-102dup NP_001159584.1:n.28-102dup
NM_001166112.2:c.28-102dup NP_001159584.1:n.28-102dup
NM_001166113.1:c.28-102dup NP_001159585.1:n.28-102dup
NM_001166114.1:c.43dup NP_001159586.1:p.Ala15GlyfsTer?
NM_006702.4:c.28-102dup NP_006693.3:n.28-102dup
NM_006702.5:c.28-102dup NP_006693.3:n.28-102dup
ENST00000221249.10:c.28-102dup ENSP00000221249.5:n.28-102dup
ENST00000414982.7:c.70dup ENSP00000407509.2:p.Ala24GlyfsTer?
ENST00000450331.7:c.28-102dup ENSP00000394348.2:n.28-102dup
ENST00000545201.6:c.28-102dup ENSP00000443323.1:n.28-102dup
ENST00000593924.5:c.28-102dup ENSP00000469794.1:n.28-102dup
ENST00000596515.5:c.28-102dup ENSP00000470461.1:n.28-102dup
ENST00000600737.5:c.43dup ENSP00000473211.1:p.Ala15GlyfsTer?
ENST00000600942.5:c.28-102dup ENSP00000472572.1:n.28-102dup
ENST00000601001.5:c.28-102dup ENSP00000472631.1:n.28-102dup
ENST00000601668.5:c.28-102dup ENSP00000470608.1:n.28-102dup
ENST00000601870.1:c.532-102dup