Canonical Allele Identifier: CA2245346641

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425535T= , CM000679.2:g.6425535T=	GRCh38
NC_000017.10:g.6328855T= , CM000679.1:g.6328855T=	GRCh37
NC_000017.9:g.6269579T=	NCBI36
NG_008474.1:g.14665A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.1080A= MANE Select	ENSP00000370521.3:p.Ala360=
ENST00000250087.9:c.891A=	ENSP00000250087.5:p.Ala297=
ENST00000381128.2:c.*952A=	ENSP00000370520.2:n.*952A=
ENST00000381129.7:c.1080A=	ENSP00000370521.3:p.Ala360=
ENST00000570466.5:c.1014A=	ENSP00000461287.1:p.Ala338=
ENST00000570584.5:c.251+8384A=
ENST00000574506.5:c.1044A=	ENSP00000458456.1:p.Ala348=
ENST00000575265.5:c.*1051A=	ENSP00000459673.1:n.*1051A=
ENST00000576307.5:c.900A=	ENSP00000459522.1:p.Ala300=
ENST00000576776.5:c.1008A=	ENSP00000460827.1:p.Ala336=
ENST00000621374.4:c.*98A=	ENSP00000481337.1:n.*98A=
NM_001033054.2:c.891A=	NP_001028226.1:p.Ala297=
NM_001033055.2:c.900A=	NP_001028227.1:p.Ala300=
NM_001285399.2:c.1044A=	NP_001272328.1:p.Ala348=
NM_001285400.2:c.1014A=	NP_001272329.1:p.Ala338=
NM_001285401.2:c.1008A=	NP_001272330.1:p.Ala336=
NM_001285402.1:c.963A=	NP_001272331.1:p.Ala321=
NM_014336.4:c.1080A=	NP_055151.3:p.Ala360=
NM_001033054.3:c.891A=	NP_001028226.1:p.Ala297=
NM_001033055.3:c.900A=	NP_001028227.1:p.Ala300=
NM_001285399.3:c.1044A=	NP_001272328.1:p.Ala348=
NM_001285400.3:c.1014A=	NP_001272329.1:p.Ala338=
NM_001285401.3:c.1008A=	NP_001272330.1:p.Ala336=
NM_001285402.2:c.963A=	NP_001272331.1:p.Ala321=
NM_001285403.3:c.*1051A=	NP_001272332.1:n.*1051A=
NM_014336.5:c.1080A= MANE Select	NP_055151.3:p.Ala360=
NM_001285403.4:c.*1051A=	NP_001272332.1:n.*1051A=