Canonical Allele Identifier: CA514856627

Gene: PNPLA3

Linked Data

• MyVariant Identifiers: chr22:g.44324706C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43928826C>G , CM000684.2:g.43928826C>G	GRCh38
NC_000022.10:g.44324706C>G , CM000684.1:g.44324706C>G	GRCh37
NC_000022.9:g.42656039C>G	NCBI36
NG_008631.1:g.10088C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216180.8:c.423C>G MANE Select	ENSP00000216180.3:p.Ala141=
ENST00000216180.7:c.423C>G	ENSP00000216180.3:p.Ala141=
ENST00000406117.6:c.*55C>G	ENSP00000384668.2:n.*55C>G
ENST00000423180.2:c.411C>G	ENSP00000397987.2:p.Ala137=
ENST00000478713.1:n.457C>G
NM_025225.2:c.423C>G	NP_079501.2:p.Ala141=
NM_025225.3:c.423C>G MANE Select	NP_079501.2:p.Ala141=