Canonical Allele Identifier: CA378978632

Gene: PNPLA2

Linked Data

• gnomAD v4: 11-821855-A-C
• MyVariant Identifiers: chr11:g.821855A>C (hg19) ; chr11:g.821855A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.821855A>C , CM000673.2:g.821855A>C	GRCh38
NC_000011.9:g.821855A>C , CM000673.1:g.821855A>C	GRCh37
NC_000011.8:g.811855A>C	NCBI36
NG_023394.1:g.7955A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336615.9:c.415A>C MANE Select	ENSP00000337701.4:p.Ile139Leu
ENST00000336615.8:c.415A>C	ENSP00000337701.4:p.Ile139Leu
ENST00000525250.5:n.1021A>C
ENST00000534561.1:n.82A>C
ENST00000617551.1:c.-836A>C	ENSP00000481602.1:n.-836A>C
NM_020376.3:c.415A>C	NP_065109.1:p.Ile139Leu
XM_006718265.2:c.415A>C	XP_006718328.1:p.Ile139Leu
XM_006718266.2:c.415A>C	XP_006718329.1:p.Ile139Leu
XM_006718265.3:c.415A>C	XP_006718328.1:p.Ile139Leu
XM_006718266.3:c.415A>C	XP_006718329.1:p.Ile139Leu
XM_017018028.1:c.415A>C	XP_016873517.1:p.Ile139Leu
XM_024448618.1:c.415A>C	XP_024304386.1:p.Ile139Leu
NM_020376.4:c.415A>C MANE Select	NP_065109.1:p.Ile139Leu