Canonical Allele Identifier: CA2245346711

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425567G= , CM000679.2:g.6425567G=	GRCh38
NC_000017.10:g.6328887G= , CM000679.1:g.6328887G=	GRCh37
NC_000017.9:g.6269611G=	NCBI36
NG_008474.1:g.14633C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1048C= MANE Select	ENSP00000370521.3:p.Pro350=
ENST00000250087.9:c.859C=	ENSP00000250087.5:p.Pro287=
ENST00000381128.2:c.*920C=	ENSP00000370520.2:n.*920C=
ENST00000381129.7:c.1048C=	ENSP00000370521.3:p.Pro350=
ENST00000570466.5:c.982C=	ENSP00000461287.1:p.Pro328=
ENST00000570584.5:c.251+8352C=
ENST00000574506.5:c.1012C=	ENSP00000458456.1:p.Pro338=
ENST00000575265.5:c.*1019C=	ENSP00000459673.1:n.*1019C=
ENST00000576307.5:c.868C=	ENSP00000459522.1:p.Pro290=
ENST00000576776.5:c.976C=	ENSP00000460827.1:p.Pro326=
ENST00000621374.4:c.*66C=	ENSP00000481337.1:n.*66C=
NM_001033054.2:c.859C=	NP_001028226.1:p.Pro287=
NM_001033055.2:c.868C=	NP_001028227.1:p.Pro290=
NM_001285399.2:c.1012C=	NP_001272328.1:p.Pro338=
NM_001285400.2:c.982C=	NP_001272329.1:p.Pro328=
NM_001285401.2:c.976C=	NP_001272330.1:p.Pro326=
NM_001285402.1:c.931C=	NP_001272331.1:p.Pro311=
NM_014336.4:c.1048C=	NP_055151.3:p.Pro350=
NM_001033054.3:c.859C=	NP_001028226.1:p.Pro287=
NM_001033055.3:c.868C=	NP_001028227.1:p.Pro290=
NM_001285399.3:c.1012C=	NP_001272328.1:p.Pro338=
NM_001285400.3:c.982C=	NP_001272329.1:p.Pro328=
NM_001285401.3:c.976C=	NP_001272330.1:p.Pro326=
NM_001285402.2:c.931C=	NP_001272331.1:p.Pro311=
NM_001285403.3:c.*1019C=	NP_001272332.1:n.*1019C=
NM_014336.5:c.1048C= MANE Select	NP_055151.3:p.Pro350=
NM_001285403.4:c.*1019C=	NP_001272332.1:n.*1019C=