Canonical Allele Identifier: CA981100138
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1911776550
gnomAD v3: 17-6425165-G-A
gnomAD v4: 17-6425165-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425165G>A , CM000679.2:g.6425165G>A GRCh38
NC_000017.10:g.6328485G>A , CM000679.1:g.6328485G>A GRCh37
NC_000017.9:g.6269209G>A NCBI36
NG_008474.1:g.15035C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.*295C>T MANE Select ENSP00000370521.3:n.*295C>T
ENST00000250087.9:c.*295C>T ENSP00000250087.5:n.*295C>T
ENST00000381128.2:c.*1322C>T ENSP00000370520.2:n.*1322C>T
ENST00000381129.7:c.*295C>T ENSP00000370521.3:n.*295C>T
ENST00000570584.5:c.251+8754C>T
ENST00000574506.5:c.*295C>T ENSP00000458456.1:n.*295C>T
NM_001033054.2:c.*295C>T NP_001028226.1:n.*295C>T
NM_001033055.2:c.*295C>T NP_001028227.1:n.*295C>T
NM_001285399.2:c.*295C>T NP_001272328.1:n.*295C>T
NM_001285400.2:c.*295C>T NP_001272329.1:n.*295C>T
NM_001285401.2:c.*295C>T NP_001272330.1:n.*295C>T
NM_001285402.1:c.*295C>T NP_001272331.1:n.*295C>T
NM_014336.4:c.*295C>T NP_055151.3:n.*295C>T
NM_001033054.3:c.*295C>T NP_001028226.1:n.*295C>T
NM_001033055.3:c.*295C>T NP_001028227.1:n.*295C>T
NM_001285399.3:c.*295C>T NP_001272328.1:n.*295C>T
NM_001285400.3:c.*295C>T NP_001272329.1:n.*295C>T
NM_001285401.3:c.*295C>T NP_001272330.1:n.*295C>T
NM_001285402.2:c.*295C>T NP_001272331.1:n.*295C>T
NM_014336.5:c.*295C>T MANE Select NP_055151.3:n.*295C>T