Canonical Allele Identifier: CA397394240
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425501T>G , CM000679.2:g.6425501T>G GRCh38
NC_000017.10:g.6328821T>G , CM000679.1:g.6328821T>G GRCh37
NC_000017.9:g.6269545T>G NCBI36
NG_008474.1:g.14699A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.1114A>C MANE Select ENSP00000370521.3:p.Thr372Pro
ENST00000250087.9:c.925A>C ENSP00000250087.5:p.Thr309Pro
ENST00000381128.2:c.*986A>C ENSP00000370520.2:n.*986A>C
ENST00000381129.7:c.1114A>C ENSP00000370521.3:p.Thr372Pro
ENST00000570466.5:c.1048A>C ENSP00000461287.1:p.Thr350Pro
ENST00000570584.5:c.251+8418A>C
ENST00000574506.5:c.1078A>C ENSP00000458456.1:p.Thr360Pro
ENST00000575265.5:c.*1085A>C ENSP00000459673.1:n.*1085A>C
ENST00000576307.5:c.934A>C ENSP00000459522.1:p.Thr312Pro
ENST00000576776.5:c.1042A>C ENSP00000460827.1:p.Thr348Pro
ENST00000621374.4:c.*132A>C ENSP00000481337.1:n.*132A>C
NM_001033054.2:c.925A>C NP_001028226.1:p.Thr309Pro
NM_001033055.2:c.934A>C NP_001028227.1:p.Thr312Pro
NM_001285399.2:c.1078A>C NP_001272328.1:p.Thr360Pro
NM_001285400.2:c.1048A>C NP_001272329.1:p.Thr350Pro
NM_001285401.2:c.1042A>C NP_001272330.1:p.Thr348Pro
NM_001285402.1:c.997A>C NP_001272331.1:p.Thr333Pro
NM_014336.4:c.1114A>C NP_055151.3:p.Thr372Pro
NM_001033054.3:c.925A>C NP_001028226.1:p.Thr309Pro
NM_001033055.3:c.934A>C NP_001028227.1:p.Thr312Pro
NM_001285399.3:c.1078A>C NP_001272328.1:p.Thr360Pro
NM_001285400.3:c.1048A>C NP_001272329.1:p.Thr350Pro
NM_001285401.3:c.1042A>C NP_001272330.1:p.Thr348Pro
NM_001285402.2:c.997A>C NP_001272331.1:p.Thr333Pro
NM_001285403.3:c.*1085A>C NP_001272332.1:n.*1085A>C
NM_014336.5:c.1114A>C MANE Select NP_055151.3:p.Thr372Pro
NM_001285403.4:c.*1085A>C NP_001272332.1:n.*1085A>C