Canonical Allele Identifier: CA1947314924

Gene: PNPLA2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.822000_822004delinsATCCC , CM000673.2:g.822000_822004delinsATCCC	GRCh38
NC_000011.9:g.822000_822004delinsATCCC , CM000673.1:g.822000_822004delinsATCCC	GRCh37
NC_000011.8:g.812000_812004delinsATCCC	NCBI36
NG_023394.1:g.8100_8104delinsATCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336615.9:c.463_467delinsATCCC MANE Select	ENSP00000337701.4:p.Ile155=
ENST00000336615.8:c.463_467delinsATCCC	ENSP00000337701.4:p.Ile155=
ENST00000525250.5:n.1069_1073delinsATCCC
ENST00000534561.1:n.130_134delinsATCCC
ENST00000617551.1:c.-788_-784delinsATCCC	ENSP00000481602.1:n.-788_-784delinsATCCC
NM_020376.3:c.463_467delinsATCCC	NP_065109.1:p.Ile155=
XM_006718265.2:c.463_467delinsATCCC	XP_006718328.1:p.Ile155=
XM_006718266.2:c.463_467delinsATCCC	XP_006718329.1:p.Ile155=
XM_006718265.3:c.463_467delinsATCCC	XP_006718328.1:p.Ile155=
XM_006718266.3:c.463_467delinsATCCC	XP_006718329.1:p.Ile155=
XM_017018028.1:c.463_467delinsATCCC	XP_016873517.1:p.Ile155=
XM_024448618.1:c.463_467delinsATCCC	XP_024304386.1:p.Ile155=
NM_020376.4:c.463_467delinsATCCC MANE Select	NP_065109.1:p.Ile155=