Canonical Allele Identifier: CA2245346824

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425618G= , CM000679.2:g.6425618G=	GRCh38
NC_000017.10:g.6328938G= , CM000679.1:g.6328938G=	GRCh37
NC_000017.9:g.6269662G=	NCBI36
NG_008474.1:g.14582C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.997C= MANE Select	ENSP00000370521.3:p.Gln333=
ENST00000250087.9:c.808C=	ENSP00000250087.5:p.Gln270=
ENST00000381128.2:c.*869C=	ENSP00000370520.2:n.*869C=
ENST00000381129.7:c.997C=	ENSP00000370521.3:p.Gln333=
ENST00000570466.5:c.931C=	ENSP00000461287.1:p.Gln311=
ENST00000570584.5:c.251+8301C=
ENST00000574506.5:c.961C=	ENSP00000458456.1:p.Gln321=
ENST00000575265.5:c.*968C=	ENSP00000459673.1:n.*968C=
ENST00000576307.5:c.817C=	ENSP00000459522.1:p.Gln273=
ENST00000576776.5:c.925C=	ENSP00000460827.1:p.Gln309=
ENST00000621374.4:c.*15C=	ENSP00000481337.1:n.*15C=
NM_001033054.2:c.808C=	NP_001028226.1:p.Gln270=
NM_001033055.2:c.817C=	NP_001028227.1:p.Gln273=
NM_001285399.2:c.961C=	NP_001272328.1:p.Gln321=
NM_001285400.2:c.931C=	NP_001272329.1:p.Gln311=
NM_001285401.2:c.925C=	NP_001272330.1:p.Gln309=
NM_001285402.1:c.880C=	NP_001272331.1:p.Gln294=
NM_014336.4:c.997C=	NP_055151.3:p.Gln333=
NM_001033054.3:c.808C=	NP_001028226.1:p.Gln270=
NM_001033055.3:c.817C=	NP_001028227.1:p.Gln273=
NM_001285399.3:c.961C=	NP_001272328.1:p.Gln321=
NM_001285400.3:c.931C=	NP_001272329.1:p.Gln311=
NM_001285401.3:c.925C=	NP_001272330.1:p.Gln309=
NM_001285402.2:c.880C=	NP_001272331.1:p.Gln294=
NM_001285403.3:c.*968C=	NP_001272332.1:n.*968C=
NM_014336.5:c.997C= MANE Select	NP_055151.3:p.Gln333=
NM_001285403.4:c.*968C=	NP_001272332.1:n.*968C=