Canonical Allele Identifier: CA2245346858
Gene: AIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425632C= , CM000679.2:g.6425632C= GRCh38
NC_000017.10:g.6328952C= , CM000679.1:g.6328952C= GRCh37
NC_000017.9:g.6269676C= NCBI36
NG_008474.1:g.14568G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.983G= MANE Select ENSP00000370521.3:p.Ser328=
ENST00000250087.9:c.794G= ENSP00000250087.5:p.Ser265=
ENST00000381128.2:c.*855G= ENSP00000370520.2:n.*855G=
ENST00000381129.7:c.983G= ENSP00000370521.3:p.Ser328=
ENST00000570466.5:c.917G= ENSP00000461287.1:p.Ser306=
ENST00000570584.5:c.251+8287G=
ENST00000574506.5:c.947G= ENSP00000458456.1:p.Ser316=
ENST00000575265.5:c.*954G= ENSP00000459673.1:n.*954G=
ENST00000576307.5:c.803G= ENSP00000459522.1:p.Ser268=
ENST00000576776.5:c.911G= ENSP00000460827.1:p.Ser304=
ENST00000621374.4:c.*1G= ENSP00000481337.1:n.*1G=
NM_001033054.2:c.794G= NP_001028226.1:p.Ser265=
NM_001033055.2:c.803G= NP_001028227.1:p.Ser268=
NM_001285399.2:c.947G= NP_001272328.1:p.Ser316=
NM_001285400.2:c.917G= NP_001272329.1:p.Ser306=
NM_001285401.2:c.911G= NP_001272330.1:p.Ser304=
NM_001285402.1:c.866G= NP_001272331.1:p.Ser289=
NM_014336.4:c.983G= NP_055151.3:p.Ser328=
NM_001033054.3:c.794G= NP_001028226.1:p.Ser265=
NM_001033055.3:c.803G= NP_001028227.1:p.Ser268=
NM_001285399.3:c.947G= NP_001272328.1:p.Ser316=
NM_001285400.3:c.917G= NP_001272329.1:p.Ser306=
NM_001285401.3:c.911G= NP_001272330.1:p.Ser304=
NM_001285402.2:c.866G= NP_001272331.1:p.Ser289=
NM_001285403.3:c.*954G= NP_001272332.1:n.*954G=
NM_014336.5:c.983G= MANE Select NP_055151.3:p.Ser328=
NM_001285403.4:c.*954G= NP_001272332.1:n.*954G=