Canonical Allele Identifier: CA403138348

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7625921G>C (hg19) ; chr19:g.7561035G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7561035G>C , CM000681.2:g.7561035G>C	GRCh38
NC_000019.9:g.7625921G>C , CM000681.1:g.7625921G>C	GRCh37
NC_000019.8:g.7531921G>C	NCBI36
NG_013374.1:g.31884G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3838G>C MANE Select	ENSP00000473211.1:p.Gly1280Arg
ENST00000221249.10:c.3724G>C	ENSP00000221249.5:p.Gly1242Arg
ENST00000414982.7:c.3868G>C	ENSP00000407509.2:p.Gly1290Arg
ENST00000450331.7:c.3724G>C	ENSP00000394348.2:p.Gly1242Arg
ENST00000545201.6:c.3643G>C	ENSP00000443323.1:p.Gly1215Arg
ENST00000597202.1:n.196G>C
ENST00000599947.1:c.207G>C
ENST00000600737.5:c.3838G>C	ENSP00000473211.1:p.Gly1280Arg
NM_001166111.1:c.3868G>C	NP_001159583.1:p.Gly1290Arg
NM_001166112.1:c.3643G>C	NP_001159584.1:p.Gly1215Arg
NM_001166113.1:c.3724G>C	NP_001159585.1:p.Gly1242Arg
NM_001166114.1:c.3838G>C	NP_001159586.1:p.Gly1280Arg
NM_006702.4:c.3724G>C	NP_006693.3:p.Gly1242Arg
NM_001166111.2:c.3868G>C	NP_001159583.1:p.Gly1290Arg
NM_001166114.2:c.3838G>C MANE Select	NP_001159586.1:p.Gly1280Arg
NM_006702.5:c.3724G>C	NP_006693.3:p.Gly1242Arg
NM_001166112.2:c.3643G>C	NP_001159584.1:p.Gly1215Arg