Canonical Allele Identifier: CA497687347
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425565T>A , CM000679.2:g.6425565T>A GRCh38
NC_000017.10:g.6328885T>A , CM000679.1:g.6328885T>A GRCh37
NC_000017.9:g.6269609T>A NCBI36
NG_008474.1:g.14635A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1050A>T MANE Select ENSP00000370521.3:p.Pro350=
ENST00000250087.9:c.861A>T ENSP00000250087.5:p.Pro287=
ENST00000381128.2:c.*922A>T ENSP00000370520.2:p.=
ENST00000381129.7:c.1050A>T ENSP00000370521.3:p.Pro350=
ENST00000570466.5:c.984A>T ENSP00000461287.1:p.Pro328=
ENST00000570584.5:n.251+8354A>T
ENST00000574506.5:c.1014A>T ENSP00000458456.1:p.Pro338=
ENST00000575265.5:c.*1021A>T ENSP00000459673.1:p.=
ENST00000576307.5:c.870A>T ENSP00000459522.1:p.Pro290=
ENST00000576776.5:c.978A>T ENSP00000460827.1:p.Pro326=
ENST00000621374.4:c.*68A>T ENSP00000481337.1:p.=
NM_001033054.2:c.861A>T NP_001028226.1:p.Pro287=
NM_001033055.2:c.870A>T NP_001028227.1:p.Pro290=
NM_001285399.2:c.1014A>T NP_001272328.1:p.Pro338=
NM_001285400.2:c.984A>T NP_001272329.1:p.Pro328=
NM_001285401.2:c.978A>T NP_001272330.1:p.Pro326=
NM_001285402.1:c.933A>T NP_001272331.1:p.Pro311=
NM_014336.4:c.1050A>T NP_055151.3:p.Pro350=
NM_001033054.3:c.861A>T NP_001028226.1:p.Pro287=
NM_001033055.3:c.870A>T NP_001028227.1:p.Pro290=
NM_001285399.3:c.1014A>T NP_001272328.1:p.Pro338=
NM_001285400.3:c.984A>T NP_001272329.1:p.Pro328=
NM_001285401.3:c.978A>T NP_001272330.1:p.Pro326=
NM_001285402.2:c.933A>T NP_001272331.1:p.Pro311=
NM_001285403.3:c.*1021A>T NP_001272332.1:p.=
NM_014336.5:c.1050A>T MANE Select NP_055151.3:p.Pro350=
NM_001285403.4:c.*1021A>T NP_001272332.1:p.=