Canonical Allele Identifier: CA5790996

Gene: PNPLA2

Linked Data

• dbSNP Id: rs753527241
• ExAC: 11:821959 C / T
• gnomAD v2: 11-821959-C-T
• MyVariant Identifiers: chr11:g.821959C>T (hg19) ; chr11:g.821959C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.821959C>T , CM000673.2:g.821959C>T	GRCh38
NC_000011.9:g.821959C>T , CM000673.1:g.821959C>T	GRCh37
NC_000011.8:g.811959C>T	NCBI36
NG_023394.1:g.8059C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336615.9:c.422C>T MANE Select	ENSP00000337701.4:p.Ala141Val
ENST00000336615.8:c.422C>T	ENSP00000337701.4:p.Ala141Val
ENST00000525250.5:n.1028C>T
ENST00000534561.1:n.89C>T
ENST00000617551.1:c.-829C>T	ENSP00000481602.1:n.-829C>T
NM_020376.3:c.422C>T	NP_065109.1:p.Ala141Val
XM_006718265.2:c.422C>T	XP_006718328.1:p.Ala141Val
XM_006718266.2:c.422C>T	XP_006718329.1:p.Ala141Val
XM_006718265.3:c.422C>T	XP_006718328.1:p.Ala141Val
XM_006718266.3:c.422C>T	XP_006718329.1:p.Ala141Val
XM_017018028.1:c.422C>T	XP_016873517.1:p.Ala141Val
XM_024448618.1:c.422C>T	XP_024304386.1:p.Ala141Val
NM_020376.4:c.422C>T MANE Select	NP_065109.1:p.Ala141Val