Canonical Allele Identifier: CA397394211
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425488G>C , CM000679.2:g.6425488G>C GRCh38
NC_000017.10:g.6328808G>C , CM000679.1:g.6328808G>C GRCh37
NC_000017.9:g.6269532G>C NCBI36
NG_008474.1:g.14712C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1127C>G MANE Select ENSP00000370521.3:p.Pro376Arg
ENST00000250087.9:c.938C>G ENSP00000250087.5:p.Pro313Arg
ENST00000381128.2:c.*999C>G ENSP00000370520.2:p.=
ENST00000381129.7:c.1127C>G ENSP00000370521.3:p.Pro376Arg
ENST00000570466.5:c.1061C>G ENSP00000461287.1:p.Pro354Arg
ENST00000570584.5:n.251+8431C>G
ENST00000574506.5:c.1091C>G ENSP00000458456.1:p.Pro364Arg
ENST00000575265.5:c.*1098C>G ENSP00000459673.1:p.=
ENST00000576307.5:c.947C>G ENSP00000459522.1:p.Pro316Arg
ENST00000576776.5:c.1055C>G ENSP00000460827.1:p.Pro352Arg
ENST00000621374.4:c.*145C>G ENSP00000481337.1:p.=
NM_001033054.2:c.938C>G NP_001028226.1:p.Pro313Arg
NM_001033055.2:c.947C>G NP_001028227.1:p.Pro316Arg
NM_001285399.2:c.1091C>G NP_001272328.1:p.Pro364Arg
NM_001285400.2:c.1061C>G NP_001272329.1:p.Pro354Arg
NM_001285401.2:c.1055C>G NP_001272330.1:p.Pro352Arg
NM_001285402.1:c.1010C>G NP_001272331.1:p.Pro337Arg
NM_014336.4:c.1127C>G NP_055151.3:p.Pro376Arg
NM_001033054.3:c.938C>G NP_001028226.1:p.Pro313Arg
NM_001033055.3:c.947C>G NP_001028227.1:p.Pro316Arg
NM_001285399.3:c.1091C>G NP_001272328.1:p.Pro364Arg
NM_001285400.3:c.1061C>G NP_001272329.1:p.Pro354Arg
NM_001285401.3:c.1055C>G NP_001272330.1:p.Pro352Arg
NM_001285402.2:c.1010C>G NP_001272331.1:p.Pro337Arg
NM_001285403.3:c.*1098C>G NP_001272332.1:p.=
NM_014336.5:c.1127C>G MANE Select NP_055151.3:p.Pro376Arg
NM_001285403.4:c.*1098C>G NP_001272332.1:p.=