Canonical Allele Identifier: CA397394554
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425658C>A , CM000679.2:g.6425658C>A GRCh38
NC_000017.10:g.6328978C>A , CM000679.1:g.6328978C>A GRCh37
NC_000017.9:g.6269702C>A NCBI36
NG_008474.1:g.14542G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.957G>T MANE Select ENSP00000370521.3:p.Glu319Asp
ENST00000250087.9:c.768G>T ENSP00000250087.5:p.Glu256Asp
ENST00000381128.2:c.*829G>T ENSP00000370520.2:n.*829G>T
ENST00000381129.7:c.957G>T ENSP00000370521.3:p.Glu319Asp
ENST00000570466.5:c.891G>T ENSP00000461287.1:p.Glu297Asp
ENST00000570584.5:c.251+8261G>T
ENST00000574506.5:c.921G>T ENSP00000458456.1:p.Glu307Asp
ENST00000575265.5:c.*928G>T ENSP00000459673.1:n.*928G>T
ENST00000576307.5:c.777G>T ENSP00000459522.1:p.Glu259Asp
ENST00000576776.5:c.885G>T ENSP00000460827.1:p.Glu295Asp
ENST00000621374.4:c.956G>T ENSP00000481337.1:p.Ser319Ile
NM_001033054.2:c.768G>T NP_001028226.1:p.Glu256Asp
NM_001033055.2:c.777G>T NP_001028227.1:p.Glu259Asp
NM_001285399.2:c.921G>T NP_001272328.1:p.Glu307Asp
NM_001285400.2:c.891G>T NP_001272329.1:p.Glu297Asp
NM_001285401.2:c.885G>T NP_001272330.1:p.Glu295Asp
NM_001285402.1:c.840G>T NP_001272331.1:p.Glu280Asp
NM_014336.4:c.957G>T NP_055151.3:p.Glu319Asp
NM_001033054.3:c.768G>T NP_001028226.1:p.Glu256Asp
NM_001033055.3:c.777G>T NP_001028227.1:p.Glu259Asp
NM_001285399.3:c.921G>T NP_001272328.1:p.Glu307Asp
NM_001285400.3:c.891G>T NP_001272329.1:p.Glu297Asp
NM_001285401.3:c.885G>T NP_001272330.1:p.Glu295Asp
NM_001285402.2:c.840G>T NP_001272331.1:p.Glu280Asp
NM_001285403.3:c.*928G>T NP_001272332.1:n.*928G>T
NM_014336.5:c.957G>T MANE Select NP_055151.3:p.Glu319Asp
NM_001285403.4:c.*928G>T NP_001272332.1:n.*928G>T