Canonical Allele Identifier: CA2245346402
Gene: AIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425404C= , CM000679.2:g.6425404C= GRCh38
NC_000017.10:g.6328724C= , CM000679.1:g.6328724C= GRCh37
NC_000017.9:g.6269448C= NCBI36
NG_008474.1:g.14796G=

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.*56G= MANE Select ENSP00000370521.3:n.*56G=
ENST00000250087.9:c.*56G= ENSP00000250087.5:n.*56G=
ENST00000381128.2:c.*1083G= ENSP00000370520.2:n.*1083G=
ENST00000381129.7:c.*56G= ENSP00000370521.3:n.*56G=
ENST00000570466.5:c.*56G= ENSP00000461287.1:n.*56G=
ENST00000570584.5:c.251+8515G=
ENST00000574506.5:c.*56G= ENSP00000458456.1:n.*56G=
ENST00000575265.5:c.*1182G= ENSP00000459673.1:n.*1182G=
ENST00000576776.5:c.*56G= ENSP00000460827.1:n.*56G=
ENST00000621374.4:c.*229G= ENSP00000481337.1:n.*229G=
NM_001033054.2:c.*56G= NP_001028226.1:n.*56G=
NM_001033055.2:c.*56G= NP_001028227.1:n.*56G=
NM_001285399.2:c.*56G= NP_001272328.1:n.*56G=
NM_001285400.2:c.*56G= NP_001272329.1:n.*56G=
NM_001285401.2:c.*56G= NP_001272330.1:n.*56G=
NM_001285402.1:c.*56G= NP_001272331.1:n.*56G=
NM_014336.4:c.*56G= NP_055151.3:n.*56G=
NM_001033054.3:c.*56G= NP_001028226.1:n.*56G=
NM_001033055.3:c.*56G= NP_001028227.1:n.*56G=
NM_001285399.3:c.*56G= NP_001272328.1:n.*56G=
NM_001285400.3:c.*56G= NP_001272329.1:n.*56G=
NM_001285401.3:c.*56G= NP_001272330.1:n.*56G=
NM_001285402.2:c.*56G= NP_001272331.1:n.*56G=
NM_001285403.3:c.*1182G= NP_001272332.1:n.*1182G=
NM_014336.5:c.*56G= MANE Select NP_055151.3:n.*56G=
NM_001285403.4:c.*1182G= NP_001272332.1:n.*1182G=