Canonical Allele Identifier: CA2245346866
Gene: AIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425639T= , CM000679.2:g.6425639T= GRCh38
NC_000017.10:g.6328959T= , CM000679.1:g.6328959T= GRCh37
NC_000017.9:g.6269683T= NCBI36
NG_008474.1:g.14561A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.976A= MANE Select ENSP00000370521.3:p.Met326=
ENST00000250087.9:c.787A= ENSP00000250087.5:p.Met263=
ENST00000381128.2:c.*848A= ENSP00000370520.2:n.*848A=
ENST00000381129.7:c.976A= ENSP00000370521.3:p.Met326=
ENST00000570466.5:c.910A= ENSP00000461287.1:p.Met304=
ENST00000570584.5:c.251+8280A=
ENST00000574506.5:c.940A= ENSP00000458456.1:p.Met314=
ENST00000575265.5:c.*947A= ENSP00000459673.1:n.*947A=
ENST00000576307.5:c.796A= ENSP00000459522.1:p.Met266=
ENST00000576776.5:c.904A= ENSP00000460827.1:p.Met302=
ENST00000621374.4:c.975A= ENSP00000481337.1:p.Thr325=
NM_001033054.2:c.787A= NP_001028226.1:p.Met263=
NM_001033055.2:c.796A= NP_001028227.1:p.Met266=
NM_001285399.2:c.940A= NP_001272328.1:p.Met314=
NM_001285400.2:c.910A= NP_001272329.1:p.Met304=
NM_001285401.2:c.904A= NP_001272330.1:p.Met302=
NM_001285402.1:c.859A= NP_001272331.1:p.Met287=
NM_014336.4:c.976A= NP_055151.3:p.Met326=
NM_001033054.3:c.787A= NP_001028226.1:p.Met263=
NM_001033055.3:c.796A= NP_001028227.1:p.Met266=
NM_001285399.3:c.940A= NP_001272328.1:p.Met314=
NM_001285400.3:c.910A= NP_001272329.1:p.Met304=
NM_001285401.3:c.904A= NP_001272330.1:p.Met302=
NM_001285402.2:c.859A= NP_001272331.1:p.Met287=
NM_001285403.3:c.*947A= NP_001272332.1:n.*947A=
NM_014336.5:c.976A= MANE Select NP_055151.3:p.Met326=
NM_001285403.4:c.*947A= NP_001272332.1:n.*947A=