Canonical Allele Identifier: CA378980003

Gene: PNPLA2

Linked Data

• MyVariant Identifiers: chr11:g.822416T>C (hg19) ; chr11:g.822416T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.822416T>C , CM000673.2:g.822416T>C	GRCh38
NC_000011.9:g.822416T>C , CM000673.1:g.822416T>C	GRCh37
NC_000011.8:g.812416T>C	NCBI36
NG_023394.1:g.8516T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336615.9:c.506T>C MANE Select	ENSP00000337701.4:p.Ile169Thr
ENST00000336615.8:c.506T>C	ENSP00000337701.4:p.Ile169Thr
ENST00000525250.5:n.1112T>C
ENST00000531923.1:n.401T>C
ENST00000617551.1:c.-745T>C	ENSP00000481602.1:n.-745T>C
NM_020376.3:c.506T>C	NP_065109.1:p.Ile169Thr
XM_006718265.2:c.506T>C	XP_006718328.1:p.Ile169Thr
XM_006718266.2:c.506T>C	XP_006718329.1:p.Ile169Thr
XM_006718265.3:c.506T>C	XP_006718328.1:p.Ile169Thr
XM_006718266.3:c.506T>C	XP_006718329.1:p.Ile169Thr
XM_017018028.1:c.506T>C	XP_016873517.1:p.Ile169Thr
XM_024448618.1:c.506T>C	XP_024304386.1:p.Ile169Thr
NM_020376.4:c.506T>C MANE Select	NP_065109.1:p.Ile169Thr