Canonical Allele Identifier: CA2635688787
Gene: AIPL1 HGNC NCBI

Linked Data

gnomAD v4: 17-6425381-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425381C>A , CM000679.2:g.6425381C>A GRCh38
NC_000017.10:g.6328701C>A , CM000679.1:g.6328701C>A GRCh37
NC_000017.9:g.6269425C>A NCBI36
NG_008474.1:g.14819G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.*79G>T MANE Select ENSP00000370521.3:n.*79G>T
ENST00000250087.9:c.*79G>T ENSP00000250087.5:n.*79G>T
ENST00000381128.2:c.*1106G>T ENSP00000370520.2:n.*1106G>T
ENST00000381129.7:c.*79G>T ENSP00000370521.3:n.*79G>T
ENST00000570584.5:c.251+8538G>T
ENST00000574506.5:c.*79G>T ENSP00000458456.1:n.*79G>T
ENST00000575265.5:c.*1205G>T ENSP00000459673.1:n.*1205G>T
NM_001033054.2:c.*79G>T NP_001028226.1:n.*79G>T
NM_001033055.2:c.*79G>T NP_001028227.1:n.*79G>T
NM_001285399.2:c.*79G>T NP_001272328.1:n.*79G>T
NM_001285400.2:c.*79G>T NP_001272329.1:n.*79G>T
NM_001285401.2:c.*79G>T NP_001272330.1:n.*79G>T
NM_001285402.1:c.*79G>T NP_001272331.1:n.*79G>T
NM_014336.4:c.*79G>T NP_055151.3:n.*79G>T
NM_001033054.3:c.*79G>T NP_001028226.1:n.*79G>T
NM_001033055.3:c.*79G>T NP_001028227.1:n.*79G>T
NM_001285399.3:c.*79G>T NP_001272328.1:n.*79G>T
NM_001285400.3:c.*79G>T NP_001272329.1:n.*79G>T
NM_001285401.3:c.*79G>T NP_001272330.1:n.*79G>T
NM_001285402.2:c.*79G>T NP_001272331.1:n.*79G>T
NM_001285403.3:c.*1205G>T NP_001272332.1:n.*1205G>T
NM_014336.5:c.*79G>T MANE Select NP_055151.3:n.*79G>T
NM_001285403.4:c.*1205G>T NP_001272332.1:n.*1205G>T