Canonical Allele Identifier: CA2611771436

Gene: PNPLA2

Linked Data

• gnomAD v4: 11-822112-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.822112C>A , CM000673.2:g.822112C>A	GRCh38
NC_000011.9:g.822112C>A , CM000673.1:g.822112C>A	GRCh37
NC_000011.8:g.812112C>A	NCBI36
NG_023394.1:g.8212C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336615.9:c.486+89C>A MANE Select	ENSP00000337701.4:n.486+89C>A
ENST00000336615.8:c.486+89C>A	ENSP00000337701.4:n.486+89C>A
ENST00000525250.5:n.1092+89C>A
ENST00000531923.1:n.97C>A
ENST00000534561.1:n.242C>A
ENST00000617551.1:c.-765+89C>A	ENSP00000481602.1:n.-765+89C>A
NM_020376.3:c.486+89C>A	NP_065109.1:n.486+89C>A
XM_006718265.2:c.486+89C>A	XP_006718328.1:n.486+89C>A
XM_006718266.2:c.486+89C>A	XP_006718329.1:n.486+89C>A
XM_006718265.3:c.486+89C>A	XP_006718328.1:n.486+89C>A
XM_006718266.3:c.486+89C>A	XP_006718329.1:n.486+89C>A
XM_017018028.1:c.486+89C>A	XP_016873517.1:n.486+89C>A
XM_024448618.1:c.486+89C>A	XP_024304386.1:n.486+89C>A
NM_020376.4:c.486+89C>A MANE Select	NP_065109.1:n.486+89C>A