Canonical Allele Identifier: CA497687313
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1297009308
gnomAD v3: 17-6425526-G-C
gnomAD v4: 17-6425526-G-C
MyVariant Identifiers: chr17:g.6328846G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425526G>C , CM000679.2:g.6425526G>C GRCh38
NC_000017.10:g.6328846G>C , CM000679.1:g.6328846G>C GRCh37
NC_000017.9:g.6269570G>C NCBI36
NG_008474.1:g.14674C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.1089C>G MANE Select ENSP00000370521.3:p.Ser363=
ENST00000250087.9:c.900C>G ENSP00000250087.5:p.Ser300=
ENST00000381128.2:c.*961C>G ENSP00000370520.2:n.*961C>G
ENST00000381129.7:c.1089C>G ENSP00000370521.3:p.Ser363=
ENST00000570466.5:c.1023C>G ENSP00000461287.1:p.Ser341=
ENST00000570584.5:c.251+8393C>G
ENST00000574506.5:c.1053C>G ENSP00000458456.1:p.Ser351=
ENST00000575265.5:c.*1060C>G ENSP00000459673.1:n.*1060C>G
ENST00000576307.5:c.909C>G ENSP00000459522.1:p.Ser303=
ENST00000576776.5:c.1017C>G ENSP00000460827.1:p.Ser339=
ENST00000621374.4:c.*107C>G ENSP00000481337.1:n.*107C>G
NM_001033054.2:c.900C>G NP_001028226.1:p.Ser300=
NM_001033055.2:c.909C>G NP_001028227.1:p.Ser303=
NM_001285399.2:c.1053C>G NP_001272328.1:p.Ser351=
NM_001285400.2:c.1023C>G NP_001272329.1:p.Ser341=
NM_001285401.2:c.1017C>G NP_001272330.1:p.Ser339=
NM_001285402.1:c.972C>G NP_001272331.1:p.Ser324=
NM_014336.4:c.1089C>G NP_055151.3:p.Ser363=
NM_001033054.3:c.900C>G NP_001028226.1:p.Ser300=
NM_001033055.3:c.909C>G NP_001028227.1:p.Ser303=
NM_001285399.3:c.1053C>G NP_001272328.1:p.Ser351=
NM_001285400.3:c.1023C>G NP_001272329.1:p.Ser341=
NM_001285401.3:c.1017C>G NP_001272330.1:p.Ser339=
NM_001285402.2:c.972C>G NP_001272331.1:p.Ser324=
NM_001285403.3:c.*1060C>G NP_001272332.1:n.*1060C>G
NM_014336.5:c.1089C>G MANE Select NP_055151.3:p.Ser363=
NM_001285403.4:c.*1060C>G NP_001272332.1:n.*1060C>G