Canonical Allele Identifier: CA2245346952

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425682G= , CM000679.2:g.6425682G=	GRCh38
NC_000017.10:g.6329002G= , CM000679.1:g.6329002G=	GRCh37
NC_000017.9:g.6269726G=	NCBI36
NG_008474.1:g.14518C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.933C= MANE Select	ENSP00000370521.3:p.Arg311=
ENST00000250087.9:c.744C=	ENSP00000250087.5:p.Arg248=
ENST00000381128.2:c.*805C=	ENSP00000370520.2:n.*805C=
ENST00000381129.7:c.933C=	ENSP00000370521.3:p.Arg311=
ENST00000570466.5:c.867C=	ENSP00000461287.1:p.Arg289=
ENST00000570584.5:c.251+8237C=
ENST00000574506.5:c.897C=	ENSP00000458456.1:p.Arg299=
ENST00000575265.5:c.*904C=	ENSP00000459673.1:n.*904C=
ENST00000576307.5:c.753C=	ENSP00000459522.1:p.Arg251=
ENST00000576776.5:c.861C=	ENSP00000460827.1:p.Arg287=
ENST00000621374.4:c.932C=	ENSP00000481337.1:p.Ala311=
NM_001033054.2:c.744C=	NP_001028226.1:p.Arg248=
NM_001033055.2:c.753C=	NP_001028227.1:p.Arg251=
NM_001285399.2:c.897C=	NP_001272328.1:p.Arg299=
NM_001285400.2:c.867C=	NP_001272329.1:p.Arg289=
NM_001285401.2:c.861C=	NP_001272330.1:p.Arg287=
NM_001285402.1:c.816C=	NP_001272331.1:p.Arg272=
NM_014336.4:c.933C=	NP_055151.3:p.Arg311=
NM_001033054.3:c.744C=	NP_001028226.1:p.Arg248=
NM_001033055.3:c.753C=	NP_001028227.1:p.Arg251=
NM_001285399.3:c.897C=	NP_001272328.1:p.Arg299=
NM_001285400.3:c.867C=	NP_001272329.1:p.Arg289=
NM_001285401.3:c.861C=	NP_001272330.1:p.Arg287=
NM_001285402.2:c.816C=	NP_001272331.1:p.Arg272=
NM_001285403.3:c.*904C=	NP_001272332.1:n.*904C=
NM_014336.5:c.933C= MANE Select	NP_055151.3:p.Arg311=
NM_001285403.4:c.*904C=	NP_001272332.1:n.*904C=