Canonical Allele Identifier: CA378979988

Gene: PNPLA2

Linked Data

• MyVariant Identifiers: chr11:g.822412G>T (hg19) ; chr11:g.822412G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.822412G>T , CM000673.2:g.822412G>T	GRCh38
NC_000011.9:g.822412G>T , CM000673.1:g.822412G>T	GRCh37
NC_000011.8:g.812412G>T	NCBI36
NG_023394.1:g.8512G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336615.9:c.502G>T MANE Select	ENSP00000337701.4:p.Gly168Cys
ENST00000336615.8:c.502G>T	ENSP00000337701.4:p.Gly168Cys
ENST00000525250.5:n.1108G>T
ENST00000531923.1:n.397G>T
ENST00000617551.1:c.-749G>T	ENSP00000481602.1:n.-749G>T
NM_020376.3:c.502G>T	NP_065109.1:p.Gly168Cys
XM_006718265.2:c.502G>T	XP_006718328.1:p.Gly168Cys
XM_006718266.2:c.502G>T	XP_006718329.1:p.Gly168Cys
XM_006718265.3:c.502G>T	XP_006718328.1:p.Gly168Cys
XM_006718266.3:c.502G>T	XP_006718329.1:p.Gly168Cys
XM_017018028.1:c.502G>T	XP_016873517.1:p.Gly168Cys
XM_024448618.1:c.502G>T	XP_024304386.1:p.Gly168Cys
NM_020376.4:c.502G>T MANE Select	NP_065109.1:p.Gly168Cys