Canonical Allele Identifier: CA378980004

Gene: PNPLA2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000336615.9:c.506T>G MANE Select	ENSP00000337701.4:p.Ile169Ser
ENST00000336615.8:c.506T>G	ENSP00000337701.4:p.Ile169Ser
ENST00000525250.5:n.1112T>G
ENST00000531923.1:n.401T>G
ENST00000617551.1:c.-745T>G	ENSP00000481602.1:n.-745T>G
NM_020376.3:c.506T>G	NP_065109.1:p.Ile169Ser
XM_006718265.2:c.506T>G	XP_006718328.1:p.Ile169Ser
XM_006718266.2:c.506T>G	XP_006718329.1:p.Ile169Ser
XM_006718265.3:c.506T>G	XP_006718328.1:p.Ile169Ser
XM_006718266.3:c.506T>G	XP_006718329.1:p.Ile169Ser
XM_017018028.1:c.506T>G	XP_016873517.1:p.Ile169Ser
XM_024448618.1:c.506T>G	XP_024304386.1:p.Ile169Ser
NM_020376.4:c.506T>G MANE Select	NP_065109.1:p.Ile169Ser