Canonical Allele Identifier: CA397394387
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425579A>T , CM000679.2:g.6425579A>T GRCh38
NC_000017.10:g.6328899A>T , CM000679.1:g.6328899A>T GRCh37
NC_000017.9:g.6269623A>T NCBI36
NG_008474.1:g.14621T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1036T>A MANE Select ENSP00000370521.3:p.Ser346Thr
ENST00000250087.9:c.847T>A ENSP00000250087.5:p.Ser283Thr
ENST00000381128.2:c.*908T>A ENSP00000370520.2:n.*908T>A
ENST00000381129.7:c.1036T>A ENSP00000370521.3:p.Ser346Thr
ENST00000570466.5:c.970T>A ENSP00000461287.1:p.Ser324Thr
ENST00000570584.5:c.251+8340T>A
ENST00000574506.5:c.1000T>A ENSP00000458456.1:p.Ser334Thr
ENST00000575265.5:c.*1007T>A ENSP00000459673.1:n.*1007T>A
ENST00000576307.5:c.856T>A ENSP00000459522.1:p.Ser286Thr
ENST00000576776.5:c.964T>A ENSP00000460827.1:p.Ser322Thr
ENST00000621374.4:c.*54T>A ENSP00000481337.1:n.*54T>A
NM_001033054.2:c.847T>A NP_001028226.1:p.Ser283Thr
NM_001033055.2:c.856T>A NP_001028227.1:p.Ser286Thr
NM_001285399.2:c.1000T>A NP_001272328.1:p.Ser334Thr
NM_001285400.2:c.970T>A NP_001272329.1:p.Ser324Thr
NM_001285401.2:c.964T>A NP_001272330.1:p.Ser322Thr
NM_001285402.1:c.919T>A NP_001272331.1:p.Ser307Thr
NM_014336.4:c.1036T>A NP_055151.3:p.Ser346Thr
NM_001033054.3:c.847T>A NP_001028226.1:p.Ser283Thr
NM_001033055.3:c.856T>A NP_001028227.1:p.Ser286Thr
NM_001285399.3:c.1000T>A NP_001272328.1:p.Ser334Thr
NM_001285400.3:c.970T>A NP_001272329.1:p.Ser324Thr
NM_001285401.3:c.964T>A NP_001272330.1:p.Ser322Thr
NM_001285402.2:c.919T>A NP_001272331.1:p.Ser307Thr
NM_001285403.3:c.*1007T>A NP_001272332.1:n.*1007T>A
NM_014336.5:c.1036T>A MANE Select NP_055151.3:p.Ser346Thr
NM_001285403.4:c.*1007T>A NP_001272332.1:n.*1007T>A