Canonical Allele Identifier: CA2245346414
Gene: AIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425416A= , CM000679.2:g.6425416A= GRCh38
NC_000017.10:g.6328736A= , CM000679.1:g.6328736A= GRCh37
NC_000017.9:g.6269460A= NCBI36
NG_008474.1:g.14784T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.*44T= MANE Select ENSP00000370521.3:n.*44T=
ENST00000250087.9:c.*44T= ENSP00000250087.5:n.*44T=
ENST00000381128.2:c.*1071T= ENSP00000370520.2:n.*1071T=
ENST00000381129.7:c.*44T= ENSP00000370521.3:n.*44T=
ENST00000570466.5:c.*44T= ENSP00000461287.1:n.*44T=
ENST00000570584.5:c.251+8503T=
ENST00000574506.5:c.*44T= ENSP00000458456.1:n.*44T=
ENST00000575265.5:c.*1170T= ENSP00000459673.1:n.*1170T=
ENST00000576307.5:c.*44T= ENSP00000459522.1:n.*44T=
ENST00000576776.5:c.*44T= ENSP00000460827.1:n.*44T=
ENST00000621374.4:c.*217T= ENSP00000481337.1:n.*217T=
NM_001033054.2:c.*44T= NP_001028226.1:n.*44T=
NM_001033055.2:c.*44T= NP_001028227.1:n.*44T=
NM_001285399.2:c.*44T= NP_001272328.1:n.*44T=
NM_001285400.2:c.*44T= NP_001272329.1:n.*44T=
NM_001285401.2:c.*44T= NP_001272330.1:n.*44T=
NM_001285402.1:c.*44T= NP_001272331.1:n.*44T=
NM_014336.4:c.*44T= NP_055151.3:n.*44T=
NM_001033054.3:c.*44T= NP_001028226.1:n.*44T=
NM_001033055.3:c.*44T= NP_001028227.1:n.*44T=
NM_001285399.3:c.*44T= NP_001272328.1:n.*44T=
NM_001285400.3:c.*44T= NP_001272329.1:n.*44T=
NM_001285401.3:c.*44T= NP_001272330.1:n.*44T=
NM_001285402.2:c.*44T= NP_001272331.1:n.*44T=
NM_001285403.3:c.*1170T= NP_001272332.1:n.*1170T=
NM_014336.5:c.*44T= MANE Select NP_055151.3:n.*44T=
NM_001285403.4:c.*1170T= NP_001272332.1:n.*1170T=