Canonical Allele Identifier: CA397394357
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425564G>T , CM000679.2:g.6425564G>T GRCh38
NC_000017.10:g.6328884G>T , CM000679.1:g.6328884G>T GRCh37
NC_000017.9:g.6269608G>T NCBI36
NG_008474.1:g.14636C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1051C>A MANE Select ENSP00000370521.3:p.Pro351Thr
ENST00000250087.9:c.862C>A ENSP00000250087.5:p.Pro288Thr
ENST00000381128.2:c.*923C>A ENSP00000370520.2:n.*923C>A
ENST00000381129.7:c.1051C>A ENSP00000370521.3:p.Pro351Thr
ENST00000570466.5:c.985C>A ENSP00000461287.1:p.Pro329Thr
ENST00000570584.5:c.251+8355C>A
ENST00000574506.5:c.1015C>A ENSP00000458456.1:p.Pro339Thr
ENST00000575265.5:c.*1022C>A ENSP00000459673.1:n.*1022C>A
ENST00000576307.5:c.871C>A ENSP00000459522.1:p.Pro291Thr
ENST00000576776.5:c.979C>A ENSP00000460827.1:p.Pro327Thr
ENST00000621374.4:c.*69C>A ENSP00000481337.1:n.*69C>A
NM_001033054.2:c.862C>A NP_001028226.1:p.Pro288Thr
NM_001033055.2:c.871C>A NP_001028227.1:p.Pro291Thr
NM_001285399.2:c.1015C>A NP_001272328.1:p.Pro339Thr
NM_001285400.2:c.985C>A NP_001272329.1:p.Pro329Thr
NM_001285401.2:c.979C>A NP_001272330.1:p.Pro327Thr
NM_001285402.1:c.934C>A NP_001272331.1:p.Pro312Thr
NM_014336.4:c.1051C>A NP_055151.3:p.Pro351Thr
NM_001033054.3:c.862C>A NP_001028226.1:p.Pro288Thr
NM_001033055.3:c.871C>A NP_001028227.1:p.Pro291Thr
NM_001285399.3:c.1015C>A NP_001272328.1:p.Pro339Thr
NM_001285400.3:c.985C>A NP_001272329.1:p.Pro329Thr
NM_001285401.3:c.979C>A NP_001272330.1:p.Pro327Thr
NM_001285402.2:c.934C>A NP_001272331.1:p.Pro312Thr
NM_001285403.3:c.*1022C>A NP_001272332.1:n.*1022C>A
NM_014336.5:c.1051C>A MANE Select NP_055151.3:p.Pro351Thr
NM_001285403.4:c.*1022C>A NP_001272332.1:n.*1022C>A