Canonical Allele Identifier: CA403129713

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7619864G>C (hg19) ; chr19:g.7554978G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7554978G>C , CM000681.2:g.7554978G>C	GRCh38
NC_000019.9:g.7619864G>C , CM000681.1:g.7619864G>C	GRCh37
NC_000019.8:g.7525864G>C	NCBI36
NG_013374.1:g.25827G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.2720G>C MANE Select	ENSP00000473211.1:p.Arg907Pro
ENST00000221249.10:c.2606G>C	ENSP00000221249.5:p.Arg869Pro
ENST00000414982.7:c.2750G>C	ENSP00000407509.2:p.Arg917Pro
ENST00000450331.7:c.2606G>C	ENSP00000394348.2:p.Arg869Pro
ENST00000545201.6:c.2525G>C	ENSP00000443323.1:p.Arg842Pro
ENST00000600737.5:c.2720G>C	ENSP00000473211.1:p.Arg907Pro
NM_001166111.1:c.2750G>C	NP_001159583.1:p.Arg917Pro
NM_001166112.1:c.2525G>C	NP_001159584.1:p.Arg842Pro
NM_001166113.1:c.2606G>C	NP_001159585.1:p.Arg869Pro
NM_001166114.1:c.2720G>C	NP_001159586.1:p.Arg907Pro
NM_006702.4:c.2606G>C	NP_006693.3:p.Arg869Pro
NM_001166111.2:c.2750G>C	NP_001159583.1:p.Arg917Pro
NM_001166114.2:c.2720G>C MANE Select	NP_001159586.1:p.Arg907Pro
NM_006702.5:c.2606G>C	NP_006693.3:p.Arg869Pro
NM_001166112.2:c.2525G>C	NP_001159584.1:p.Arg842Pro