Canonical Allele Identifier: CA2245346428

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425422C= , CM000679.2:g.6425422C=	GRCh38
NC_000017.10:g.6328742C= , CM000679.1:g.6328742C=	GRCh37
NC_000017.9:g.6269466C=	NCBI36
NG_008474.1:g.14778G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.*38G= MANE Select	ENSP00000370521.3:n.*38G=
ENST00000250087.9:c.*38G=	ENSP00000250087.5:n.*38G=
ENST00000381128.2:c.*1065G=	ENSP00000370520.2:n.*1065G=
ENST00000381129.7:c.*38G=	ENSP00000370521.3:n.*38G=
ENST00000570466.5:c.*38G=	ENSP00000461287.1:n.*38G=
ENST00000570584.5:c.251+8497G=
ENST00000574506.5:c.*38G=	ENSP00000458456.1:n.*38G=
ENST00000575265.5:c.*1164G=	ENSP00000459673.1:n.*1164G=
ENST00000576307.5:c.*38G=	ENSP00000459522.1:n.*38G=
ENST00000576776.5:c.*38G=	ENSP00000460827.1:n.*38G=
ENST00000621374.4:c.*211G=	ENSP00000481337.1:n.*211G=
NM_001033054.2:c.*38G=	NP_001028226.1:n.*38G=
NM_001033055.2:c.*38G=	NP_001028227.1:n.*38G=
NM_001285399.2:c.*38G=	NP_001272328.1:n.*38G=
NM_001285400.2:c.*38G=	NP_001272329.1:n.*38G=
NM_001285401.2:c.*38G=	NP_001272330.1:n.*38G=
NM_001285402.1:c.*38G=	NP_001272331.1:n.*38G=
NM_014336.4:c.*38G=	NP_055151.3:n.*38G=
NM_001033054.3:c.*38G=	NP_001028226.1:n.*38G=
NM_001033055.3:c.*38G=	NP_001028227.1:n.*38G=
NM_001285399.3:c.*38G=	NP_001272328.1:n.*38G=
NM_001285400.3:c.*38G=	NP_001272329.1:n.*38G=
NM_001285401.3:c.*38G=	NP_001272330.1:n.*38G=
NM_001285402.2:c.*38G=	NP_001272331.1:n.*38G=
NM_001285403.3:c.*1164G=	NP_001272332.1:n.*1164G=
NM_014336.5:c.*38G= MANE Select	NP_055151.3:n.*38G=
NM_001285403.4:c.*1164G=	NP_001272332.1:n.*1164G=