Canonical Allele Identifier: CA2245346138
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1911780674
gnomAD v4: 17-6425234-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425234T>C , CM000679.2:g.6425234T>C GRCh38
NC_000017.10:g.6328554T>C , CM000679.1:g.6328554T>C GRCh37
NC_000017.9:g.6269278T>C NCBI36
NG_008474.1:g.14966A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.*226A>G MANE Select ENSP00000370521.3:n.*226A>G
ENST00000250087.9:c.*226A>G ENSP00000250087.5:n.*226A>G
ENST00000381128.2:c.*1253A>G ENSP00000370520.2:n.*1253A>G
ENST00000381129.7:c.*226A>G ENSP00000370521.3:n.*226A>G
ENST00000570584.5:c.251+8685A>G
ENST00000574506.5:c.*226A>G ENSP00000458456.1:n.*226A>G
NM_001033054.2:c.*226A>G NP_001028226.1:n.*226A>G
NM_001033055.2:c.*226A>G NP_001028227.1:n.*226A>G
NM_001285399.2:c.*226A>G NP_001272328.1:n.*226A>G
NM_001285400.2:c.*226A>G NP_001272329.1:n.*226A>G
NM_001285401.2:c.*226A>G NP_001272330.1:n.*226A>G
NM_001285402.1:c.*226A>G NP_001272331.1:n.*226A>G
NM_014336.4:c.*226A>G NP_055151.3:n.*226A>G
NM_001033054.3:c.*226A>G NP_001028226.1:n.*226A>G
NM_001033055.3:c.*226A>G NP_001028227.1:n.*226A>G
NM_001285399.3:c.*226A>G NP_001272328.1:n.*226A>G
NM_001285400.3:c.*226A>G NP_001272329.1:n.*226A>G
NM_001285401.3:c.*226A>G NP_001272330.1:n.*226A>G
NM_001285402.2:c.*226A>G NP_001272331.1:n.*226A>G
NM_014336.5:c.*226A>G MANE Select NP_055151.3:n.*226A>G