Canonical Allele Identifier: CA378978731

Gene: PNPLA2

Linked Data

• gnomAD v4: 11-821964-G-A
• MyVariant Identifiers: chr11:g.821964G>A (hg19) ; chr11:g.821964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.821964G>A , CM000673.2:g.821964G>A	GRCh38
NC_000011.9:g.821964G>A , CM000673.1:g.821964G>A	GRCh37
NC_000011.8:g.811964G>A	NCBI36
NG_023394.1:g.8064G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336615.9:c.427G>A MANE Select	ENSP00000337701.4:p.Val143Ile
ENST00000336615.8:c.427G>A	ENSP00000337701.4:p.Val143Ile
ENST00000525250.5:n.1033G>A
ENST00000534561.1:n.94G>A
ENST00000617551.1:c.-824G>A	ENSP00000481602.1:n.-824G>A
NM_020376.3:c.427G>A	NP_065109.1:p.Val143Ile
XM_006718265.2:c.427G>A	XP_006718328.1:p.Val143Ile
XM_006718266.2:c.427G>A	XP_006718329.1:p.Val143Ile
XM_006718265.3:c.427G>A	XP_006718328.1:p.Val143Ile
XM_006718266.3:c.427G>A	XP_006718329.1:p.Val143Ile
XM_017018028.1:c.427G>A	XP_016873517.1:p.Val143Ile
XM_024448618.1:c.427G>A	XP_024304386.1:p.Val143Ile
NM_020376.4:c.427G>A MANE Select	NP_065109.1:p.Val143Ile