Canonical Allele Identifier: CA403129614

Gene: PNPLA6

Linked Data

• gnomAD v4: 19-7554961-G-T
• MyVariant Identifiers: chr19:g.7619847G>T (hg19) ; chr19:g.7554961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7554961G>T , CM000681.2:g.7554961G>T	GRCh38
NC_000019.9:g.7619847G>T , CM000681.1:g.7619847G>T	GRCh37
NC_000019.8:g.7525847G>T	NCBI36
NG_013374.1:g.25810G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.2703G>T MANE Select	ENSP00000473211.1:p.Glu901Asp
ENST00000221249.10:c.2589G>T	ENSP00000221249.5:p.Glu863Asp
ENST00000414982.7:c.2733G>T	ENSP00000407509.2:p.Glu911Asp
ENST00000450331.7:c.2589G>T	ENSP00000394348.2:p.Glu863Asp
ENST00000545201.6:c.2508G>T	ENSP00000443323.1:p.Glu836Asp
ENST00000600737.5:c.2703G>T	ENSP00000473211.1:p.Glu901Asp
NM_001166111.1:c.2733G>T	NP_001159583.1:p.Glu911Asp
NM_001166112.1:c.2508G>T	NP_001159584.1:p.Glu836Asp
NM_001166113.1:c.2589G>T	NP_001159585.1:p.Glu863Asp
NM_001166114.1:c.2703G>T	NP_001159586.1:p.Glu901Asp
NM_006702.4:c.2589G>T	NP_006693.3:p.Glu863Asp
NM_001166111.2:c.2733G>T	NP_001159583.1:p.Glu911Asp
NM_001166114.2:c.2703G>T MANE Select	NP_001159586.1:p.Glu901Asp
NM_006702.5:c.2589G>T	NP_006693.3:p.Glu863Asp
NM_001166112.2:c.2508G>T	NP_001159584.1:p.Glu836Asp