Canonical Allele Identifier: CA497687320
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1597325043
MyVariant Identifiers: chr17:g.6328855T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425535T>C , CM000679.2:g.6425535T>C GRCh38
NC_000017.10:g.6328855T>C , CM000679.1:g.6328855T>C GRCh37
NC_000017.9:g.6269579T>C NCBI36
NG_008474.1:g.14665A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.1080A>G MANE Select ENSP00000370521.3:p.Ala360=
ENST00000250087.9:c.891A>G ENSP00000250087.5:p.Ala297=
ENST00000381128.2:c.*952A>G ENSP00000370520.2:n.*952A>G
ENST00000381129.7:c.1080A>G ENSP00000370521.3:p.Ala360=
ENST00000570466.5:c.1014A>G ENSP00000461287.1:p.Ala338=
ENST00000570584.5:c.251+8384A>G
ENST00000574506.5:c.1044A>G ENSP00000458456.1:p.Ala348=
ENST00000575265.5:c.*1051A>G ENSP00000459673.1:n.*1051A>G
ENST00000576307.5:c.900A>G ENSP00000459522.1:p.Ala300=
ENST00000576776.5:c.1008A>G ENSP00000460827.1:p.Ala336=
ENST00000621374.4:c.*98A>G ENSP00000481337.1:n.*98A>G
NM_001033054.2:c.891A>G NP_001028226.1:p.Ala297=
NM_001033055.2:c.900A>G NP_001028227.1:p.Ala300=
NM_001285399.2:c.1044A>G NP_001272328.1:p.Ala348=
NM_001285400.2:c.1014A>G NP_001272329.1:p.Ala338=
NM_001285401.2:c.1008A>G NP_001272330.1:p.Ala336=
NM_001285402.1:c.963A>G NP_001272331.1:p.Ala321=
NM_014336.4:c.1080A>G NP_055151.3:p.Ala360=
NM_001033054.3:c.891A>G NP_001028226.1:p.Ala297=
NM_001033055.3:c.900A>G NP_001028227.1:p.Ala300=
NM_001285399.3:c.1044A>G NP_001272328.1:p.Ala348=
NM_001285400.3:c.1014A>G NP_001272329.1:p.Ala338=
NM_001285401.3:c.1008A>G NP_001272330.1:p.Ala336=
NM_001285402.2:c.963A>G NP_001272331.1:p.Ala321=
NM_001285403.3:c.*1051A>G NP_001272332.1:n.*1051A>G
NM_014336.5:c.1080A>G MANE Select NP_055151.3:p.Ala360=
NM_001285403.4:c.*1051A>G NP_001272332.1:n.*1051A>G