Canonical Allele Identifier: CA2245346612

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425525C= , CM000679.2:g.6425525C=	GRCh38
NC_000017.10:g.6328845C= , CM000679.1:g.6328845C=	GRCh37
NC_000017.9:g.6269569C=	NCBI36
NG_008474.1:g.14675G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.1090G= MANE Select	ENSP00000370521.3:p.Ala364=
ENST00000250087.9:c.901G=	ENSP00000250087.5:p.Ala301=
ENST00000381128.2:c.*962G=	ENSP00000370520.2:n.*962G=
ENST00000381129.7:c.1090G=	ENSP00000370521.3:p.Ala364=
ENST00000570466.5:c.1024G=	ENSP00000461287.1:p.Ala342=
ENST00000570584.5:c.251+8394G=
ENST00000574506.5:c.1054G=	ENSP00000458456.1:p.Ala352=
ENST00000575265.5:c.*1061G=	ENSP00000459673.1:n.*1061G=
ENST00000576307.5:c.910G=	ENSP00000459522.1:p.Ala304=
ENST00000576776.5:c.1018G=	ENSP00000460827.1:p.Ala340=
ENST00000621374.4:c.*108G=	ENSP00000481337.1:n.*108G=
NM_001033054.2:c.901G=	NP_001028226.1:p.Ala301=
NM_001033055.2:c.910G=	NP_001028227.1:p.Ala304=
NM_001285399.2:c.1054G=	NP_001272328.1:p.Ala352=
NM_001285400.2:c.1024G=	NP_001272329.1:p.Ala342=
NM_001285401.2:c.1018G=	NP_001272330.1:p.Ala340=
NM_001285402.1:c.973G=	NP_001272331.1:p.Ala325=
NM_014336.4:c.1090G=	NP_055151.3:p.Ala364=
NM_001033054.3:c.901G=	NP_001028226.1:p.Ala301=
NM_001033055.3:c.910G=	NP_001028227.1:p.Ala304=
NM_001285399.3:c.1054G=	NP_001272328.1:p.Ala352=
NM_001285400.3:c.1024G=	NP_001272329.1:p.Ala342=
NM_001285401.3:c.1018G=	NP_001272330.1:p.Ala340=
NM_001285402.2:c.973G=	NP_001272331.1:p.Ala325=
NM_001285403.3:c.*1061G=	NP_001272332.1:n.*1061G=
NM_014336.5:c.1090G= MANE Select	NP_055151.3:p.Ala364=
NM_001285403.4:c.*1061G=	NP_001272332.1:n.*1061G=