Canonical Allele Identifier: CA5791033
Community Standard Title: NM_020376.4(PNPLA2):c.492C>T (p.Tyr164=)
Gene: PNPLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.822402C>T , CM000673.2:g.822402C>T GRCh38
NC_000011.9:g.822402C>T , CM000673.1:g.822402C>T GRCh37
NC_000011.8:g.812402C>T NCBI36
NG_023394.1:g.8502C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020376.4:c.492C>T MANE Select NP_065109.1:p.Tyr164=
ENST00000336615.9:c.492C>T MANE Select ENSP00000337701.4:p.Tyr164=
NM_020376.3:c.492C>T NP_065109.1:p.Tyr164=
ENST00000336615.8:c.492C>T ENSP00000337701.4:p.Tyr164=
ENST00000525250.5:n.1098C>T
ENST00000531923.1:n.387C>T
ENST00000617551.1:c.-759C>T ENSP00000481602.1:n.-759C>T
XM_006718265.2:c.492C>T XP_006718328.1:p.Tyr164=
XM_006718265.3:c.492C>T XP_006718328.1:p.Tyr164=
XM_006718266.2:c.492C>T XP_006718329.1:p.Tyr164=
XM_006718266.3:c.492C>T XP_006718329.1:p.Tyr164=
XM_017018028.1:c.492C>T XP_016873517.1:p.Tyr164=
XM_024448618.1:c.492C>T XP_024304386.1:p.Tyr164=