Canonical Allele Identifier: CA397394925
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425828T>A , CM000679.2:g.6425828T>A GRCh38
NC_000017.10:g.6329148T>A , CM000679.1:g.6329148T>A GRCh37
NC_000017.9:g.6269872T>A NCBI36
NG_008474.1:g.14372A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.787A>T MANE Select ENSP00000370521.3:p.Ile263Phe
ENST00000250087.9:c.598A>T ENSP00000250087.5:p.Ile200Phe
ENST00000381128.2:c.*659A>T ENSP00000370520.2:n.*659A>T
ENST00000381129.7:c.787A>T ENSP00000370521.3:p.Ile263Phe
ENST00000570466.5:c.721A>T ENSP00000461287.1:p.Ile241Phe
ENST00000570584.5:c.251+8091A>T
ENST00000574506.5:c.751A>T ENSP00000458456.1:p.Ile251Phe
ENST00000575265.5:c.*758A>T ENSP00000459673.1:n.*758A>T
ENST00000576307.5:c.607A>T ENSP00000459522.1:p.Ile203Phe
ENST00000576776.5:c.715A>T ENSP00000460827.1:p.Ile239Phe
ENST00000621374.4:c.787A>T ENSP00000481337.1:p.Ile263Phe
NM_001033054.2:c.598A>T NP_001028226.1:p.Ile200Phe
NM_001033055.2:c.607A>T NP_001028227.1:p.Ile203Phe
NM_001285399.2:c.751A>T NP_001272328.1:p.Ile251Phe
NM_001285400.2:c.721A>T NP_001272329.1:p.Ile241Phe
NM_001285401.2:c.715A>T NP_001272330.1:p.Ile239Phe
NM_001285402.1:c.670A>T NP_001272331.1:p.Ile224Phe
NM_014336.4:c.787A>T NP_055151.3:p.Ile263Phe
NM_001033054.3:c.598A>T NP_001028226.1:p.Ile200Phe
NM_001033055.3:c.607A>T NP_001028227.1:p.Ile203Phe
NM_001285399.3:c.751A>T NP_001272328.1:p.Ile251Phe
NM_001285400.3:c.721A>T NP_001272329.1:p.Ile241Phe
NM_001285401.3:c.715A>T NP_001272330.1:p.Ile239Phe
NM_001285402.2:c.670A>T NP_001272331.1:p.Ile224Phe
NM_001285403.3:c.*758A>T NP_001272332.1:n.*758A>T
NM_014336.5:c.787A>T MANE Select NP_055151.3:p.Ile263Phe
NM_001285403.4:c.*758A>T NP_001272332.1:n.*758A>T