Canonical Allele Identifier: CA216969079

Gene: PNPLA2

Linked Data

• dbSNP Id: rs148948764
• MyVariant Identifiers: chr11:g.822310_822315del (hg19) ; chr11:g.822310_822315del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.822310_822315del , CM000673.2:g.822310_822315del	GRCh38
NC_000011.9:g.822310_822315del , CM000673.1:g.822310_822315del	GRCh37
NC_000011.8:g.812310_812315del	NCBI36
NG_023394.1:g.8410_8415del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336615.9:c.487-87_487-82del MANE Select	ENSP00000337701.4:n.487-87_487-82del
ENST00000336615.8:c.487-87_487-82del	ENSP00000337701.4:n.487-87_487-82del
ENST00000525250.5:n.1093-87_1093-82del
ENST00000531923.1:n.295_300del
ENST00000617551.1:c.-764-87_-764-82del	ENSP00000481602.1:n.-764-87_-764-82del
NM_020376.3:c.487-87_487-82del	NP_065109.1:n.487-87_487-82del
XM_006718265.2:c.487-87_487-82del	XP_006718328.1:n.487-87_487-82del
XM_006718266.2:c.487-87_487-82del	XP_006718329.1:n.487-87_487-82del
XM_006718265.3:c.487-87_487-82del	XP_006718328.1:n.487-87_487-82del
XM_006718266.3:c.487-87_487-82del	XP_006718329.1:n.487-87_487-82del
XM_017018028.1:c.487-87_487-82del	XP_016873517.1:n.487-87_487-82del
XM_024448618.1:c.487-87_487-82del	XP_024304386.1:n.487-87_487-82del
NM_020376.4:c.487-87_487-82del MANE Select	NP_065109.1:n.487-87_487-82del