Canonical Allele Identifier: CA378978627

Gene: PNPLA2

Linked Data

• MyVariant Identifiers: chr11:g.821853T>C (hg19) ; chr11:g.821853T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.821853T>C , CM000673.2:g.821853T>C	GRCh38
NC_000011.9:g.821853T>C , CM000673.1:g.821853T>C	GRCh37
NC_000011.8:g.811853T>C	NCBI36
NG_023394.1:g.7953T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336615.9:c.413T>C MANE Select	ENSP00000337701.4:p.Leu138Pro
ENST00000336615.8:c.413T>C	ENSP00000337701.4:p.Leu138Pro
ENST00000525250.5:n.1019T>C
ENST00000534561.1:n.80T>C
ENST00000617551.1:c.-838T>C	ENSP00000481602.1:n.-838T>C
NM_020376.3:c.413T>C	NP_065109.1:p.Leu138Pro
XM_006718265.2:c.413T>C	XP_006718328.1:p.Leu138Pro
XM_006718266.2:c.413T>C	XP_006718329.1:p.Leu138Pro
XM_006718265.3:c.413T>C	XP_006718328.1:p.Leu138Pro
XM_006718266.3:c.413T>C	XP_006718329.1:p.Leu138Pro
XM_017018028.1:c.413T>C	XP_016873517.1:p.Leu138Pro
XM_024448618.1:c.413T>C	XP_024304386.1:p.Leu138Pro
NM_020376.4:c.413T>C MANE Select	NP_065109.1:p.Leu138Pro