Canonical Allele Identifier: CA2320979556

Gene: PNPLA6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561132C= , CM000681.2:g.7561132C=	GRCh38
NC_000019.9:g.7626018C= , CM000681.1:g.7626018C=	GRCh37
NC_000019.8:g.7532018C=	NCBI36
NG_013374.1:g.31981C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3913+22C= MANE Select	ENSP00000473211.1:n.3913+22C=
ENST00000221249.10:c.3799+22C=	ENSP00000221249.5:n.3799+22C=
ENST00000414982.7:c.3943+22C=	ENSP00000407509.2:n.3943+22C=
ENST00000450331.7:c.3799+22C=	ENSP00000394348.2:n.3799+22C=
ENST00000545201.6:c.3718+22C=	ENSP00000443323.1:n.3718+22C=
ENST00000597202.1:n.271+22C=
ENST00000599947.1:c.282+22C=
ENST00000600737.5:c.3913+22C=	ENSP00000473211.1:n.3913+22C=
NM_001166111.1:c.3943+22C=	NP_001159583.1:n.3943+22C=
NM_001166112.1:c.3718+22C=	NP_001159584.1:n.3718+22C=
NM_001166113.1:c.3799+22C=	NP_001159585.1:n.3799+22C=
NM_001166114.1:c.3913+22C=	NP_001159586.1:n.3913+22C=
NM_006702.4:c.3799+22C=	NP_006693.3:n.3799+22C=
NM_001166111.2:c.3943+22C=	NP_001159583.1:n.3943+22C=
NM_001166114.2:c.3913+22C= MANE Select	NP_001159586.1:n.3913+22C=
NM_006702.5:c.3799+22C=	NP_006693.3:n.3799+22C=
NM_001166112.2:c.3718+22C=	NP_001159584.1:n.3718+22C=