Canonical Allele Identifier: CA2245346492
Gene: AIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425473G= , CM000679.2:g.6425473G= GRCh38
NC_000017.10:g.6328793G= , CM000679.1:g.6328793G= GRCh37
NC_000017.9:g.6269517G= NCBI36
NG_008474.1:g.14727C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1142C= MANE Select ENSP00000370521.3:p.Ser381=
ENST00000250087.9:c.953C= ENSP00000250087.5:p.Ser318=
ENST00000381128.2:c.*1014C= ENSP00000370520.2:p.=
ENST00000381129.7:c.1142C= ENSP00000370521.3:p.Ser381=
ENST00000570466.5:c.1076C= ENSP00000461287.1:p.Ser359=
ENST00000570584.5:n.251+8446C=
ENST00000574506.5:c.1106C= ENSP00000458456.1:p.Ser369=
ENST00000575265.5:c.*1113C= ENSP00000459673.1:p.=
ENST00000576307.5:c.962C= ENSP00000459522.1:p.Ser321=
ENST00000576776.5:c.1070C= ENSP00000460827.1:p.Ser357=
ENST00000621374.4:c.*160C= ENSP00000481337.1:p.=
NM_001033054.2:c.953C= NP_001028226.1:p.Ser318=
NM_001033055.2:c.962C= NP_001028227.1:p.Ser321=
NM_001285399.2:c.1106C= NP_001272328.1:p.Ser369=
NM_001285400.2:c.1076C= NP_001272329.1:p.Ser359=
NM_001285401.2:c.1070C= NP_001272330.1:p.Ser357=
NM_001285402.1:c.1025C= NP_001272331.1:p.Ser342=
NM_014336.4:c.1142C= NP_055151.3:p.Ser381=
NM_001033054.3:c.953C= NP_001028226.1:p.Ser318=
NM_001033055.3:c.962C= NP_001028227.1:p.Ser321=
NM_001285399.3:c.1106C= NP_001272328.1:p.Ser369=
NM_001285400.3:c.1076C= NP_001272329.1:p.Ser359=
NM_001285401.3:c.1070C= NP_001272330.1:p.Ser357=
NM_001285402.2:c.1025C= NP_001272331.1:p.Ser342=
NM_001285403.3:c.*1113C= NP_001272332.1:p.=
NM_014336.5:c.1142C= MANE Select NP_055151.3:p.Ser381=
NM_001285403.4:c.*1113C= NP_001272332.1:p.=