Canonical Allele Identifier: CA2635688639
Gene: AIPL1 HGNC NCBI

Linked Data

gnomAD v4: 17-6425272-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425272C>A , CM000679.2:g.6425272C>A GRCh38
NC_000017.10:g.6328592C>A , CM000679.1:g.6328592C>A GRCh37
NC_000017.9:g.6269316C>A NCBI36
NG_008474.1:g.14928G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.*188G>T MANE Select ENSP00000370521.3:n.*188G>T
ENST00000250087.9:c.*188G>T ENSP00000250087.5:n.*188G>T
ENST00000381128.2:c.*1215G>T ENSP00000370520.2:n.*1215G>T
ENST00000381129.7:c.*188G>T ENSP00000370521.3:n.*188G>T
ENST00000570584.5:c.251+8647G>T
ENST00000574506.5:c.*188G>T ENSP00000458456.1:n.*188G>T
NM_001033054.2:c.*188G>T NP_001028226.1:n.*188G>T
NM_001033055.2:c.*188G>T NP_001028227.1:n.*188G>T
NM_001285399.2:c.*188G>T NP_001272328.1:n.*188G>T
NM_001285400.2:c.*188G>T NP_001272329.1:n.*188G>T
NM_001285401.2:c.*188G>T NP_001272330.1:n.*188G>T
NM_001285402.1:c.*188G>T NP_001272331.1:n.*188G>T
NM_014336.4:c.*188G>T NP_055151.3:n.*188G>T
NM_001033054.3:c.*188G>T NP_001028226.1:n.*188G>T
NM_001033055.3:c.*188G>T NP_001028227.1:n.*188G>T
NM_001285399.3:c.*188G>T NP_001272328.1:n.*188G>T
NM_001285400.3:c.*188G>T NP_001272329.1:n.*188G>T
NM_001285401.3:c.*188G>T NP_001272330.1:n.*188G>T
NM_001285402.2:c.*188G>T NP_001272331.1:n.*188G>T
NM_014336.5:c.*188G>T MANE Select NP_055151.3:n.*188G>T
NM_001285403.4:c.*1314G>T NP_001272332.1:n.*1314G>T