Canonical Allele Identifier: CA2245346332
Gene: AIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425324T= , CM000679.2:g.6425324T= GRCh38
NC_000017.10:g.6328644T= , CM000679.1:g.6328644T= GRCh37
NC_000017.9:g.6269368T= NCBI36
NG_008474.1:g.14876A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.*136A= MANE Select ENSP00000370521.3:n.*136A=
ENST00000250087.9:c.*136A= ENSP00000250087.5:n.*136A=
ENST00000381128.2:c.*1163A= ENSP00000370520.2:n.*1163A=
ENST00000381129.7:c.*136A= ENSP00000370521.3:n.*136A=
ENST00000570584.5:c.251+8595A=
ENST00000574506.5:c.*136A= ENSP00000458456.1:n.*136A=
ENST00000575265.5:c.*1262A= ENSP00000459673.1:n.*1262A=
NM_001033054.2:c.*136A= NP_001028226.1:n.*136A=
NM_001033055.2:c.*136A= NP_001028227.1:n.*136A=
NM_001285399.2:c.*136A= NP_001272328.1:n.*136A=
NM_001285400.2:c.*136A= NP_001272329.1:n.*136A=
NM_001285401.2:c.*136A= NP_001272330.1:n.*136A=
NM_001285402.1:c.*136A= NP_001272331.1:n.*136A=
NM_014336.4:c.*136A= NP_055151.3:n.*136A=
NM_001033054.3:c.*136A= NP_001028226.1:n.*136A=
NM_001033055.3:c.*136A= NP_001028227.1:n.*136A=
NM_001285399.3:c.*136A= NP_001272328.1:n.*136A=
NM_001285400.3:c.*136A= NP_001272329.1:n.*136A=
NM_001285401.3:c.*136A= NP_001272330.1:n.*136A=
NM_001285402.2:c.*136A= NP_001272331.1:n.*136A=
NM_001285403.3:c.*1262A= NP_001272332.1:n.*1262A=
NM_014336.5:c.*136A= MANE Select NP_055151.3:n.*136A=
NM_001285403.4:c.*1262A= NP_001272332.1:n.*1262A=