Canonical Allele Identifier: CA397394185
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425474A>T , CM000679.2:g.6425474A>T GRCh38
NC_000017.10:g.6328794A>T , CM000679.1:g.6328794A>T GRCh37
NC_000017.9:g.6269518A>T NCBI36
NG_008474.1:g.14726T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1141T>A MANE Select ENSP00000370521.3:p.Ser381Thr
ENST00000250087.9:c.952T>A ENSP00000250087.5:p.Ser318Thr
ENST00000381128.2:c.*1013T>A ENSP00000370520.2:n.*1013T>A
ENST00000381129.7:c.1141T>A ENSP00000370521.3:p.Ser381Thr
ENST00000570466.5:c.1075T>A ENSP00000461287.1:p.Ser359Thr
ENST00000570584.5:c.251+8445T>A
ENST00000574506.5:c.1105T>A ENSP00000458456.1:p.Ser369Thr
ENST00000575265.5:c.*1112T>A ENSP00000459673.1:n.*1112T>A
ENST00000576307.5:c.961T>A ENSP00000459522.1:p.Ser321Thr
ENST00000576776.5:c.1069T>A ENSP00000460827.1:p.Ser357Thr
ENST00000621374.4:c.*159T>A ENSP00000481337.1:n.*159T>A
NM_001033054.2:c.952T>A NP_001028226.1:p.Ser318Thr
NM_001033055.2:c.961T>A NP_001028227.1:p.Ser321Thr
NM_001285399.2:c.1105T>A NP_001272328.1:p.Ser369Thr
NM_001285400.2:c.1075T>A NP_001272329.1:p.Ser359Thr
NM_001285401.2:c.1069T>A NP_001272330.1:p.Ser357Thr
NM_001285402.1:c.1024T>A NP_001272331.1:p.Ser342Thr
NM_014336.4:c.1141T>A NP_055151.3:p.Ser381Thr
NM_001033054.3:c.952T>A NP_001028226.1:p.Ser318Thr
NM_001033055.3:c.961T>A NP_001028227.1:p.Ser321Thr
NM_001285399.3:c.1105T>A NP_001272328.1:p.Ser369Thr
NM_001285400.3:c.1075T>A NP_001272329.1:p.Ser359Thr
NM_001285401.3:c.1069T>A NP_001272330.1:p.Ser357Thr
NM_001285402.2:c.1024T>A NP_001272331.1:p.Ser342Thr
NM_001285403.3:c.*1112T>A NP_001272332.1:n.*1112T>A
NM_014336.5:c.1141T>A MANE Select NP_055151.3:p.Ser381Thr
NM_001285403.4:c.*1112T>A NP_001272332.1:n.*1112T>A