Canonical Allele Identifier: CA2245346693

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425562A= , CM000679.2:g.6425562A=	GRCh38
NC_000017.10:g.6328882A= , CM000679.1:g.6328882A=	GRCh37
NC_000017.9:g.6269606A=	NCBI36
NG_008474.1:g.14638T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1053T= MANE Select	ENSP00000370521.3:p.Pro351=
ENST00000250087.9:c.864T=	ENSP00000250087.5:p.Pro288=
ENST00000381128.2:c.*925T=	ENSP00000370520.2:n.*925T=
ENST00000381129.7:c.1053T=	ENSP00000370521.3:p.Pro351=
ENST00000570466.5:c.987T=	ENSP00000461287.1:p.Pro329=
ENST00000570584.5:c.251+8357T=
ENST00000574506.5:c.1017T=	ENSP00000458456.1:p.Pro339=
ENST00000575265.5:c.*1024T=	ENSP00000459673.1:n.*1024T=
ENST00000576307.5:c.873T=	ENSP00000459522.1:p.Pro291=
ENST00000576776.5:c.981T=	ENSP00000460827.1:p.Pro327=
ENST00000621374.4:c.*71T=	ENSP00000481337.1:n.*71T=
NM_001033054.2:c.864T=	NP_001028226.1:p.Pro288=
NM_001033055.2:c.873T=	NP_001028227.1:p.Pro291=
NM_001285399.2:c.1017T=	NP_001272328.1:p.Pro339=
NM_001285400.2:c.987T=	NP_001272329.1:p.Pro329=
NM_001285401.2:c.981T=	NP_001272330.1:p.Pro327=
NM_001285402.1:c.936T=	NP_001272331.1:p.Pro312=
NM_014336.4:c.1053T=	NP_055151.3:p.Pro351=
NM_001033054.3:c.864T=	NP_001028226.1:p.Pro288=
NM_001033055.3:c.873T=	NP_001028227.1:p.Pro291=
NM_001285399.3:c.1017T=	NP_001272328.1:p.Pro339=
NM_001285400.3:c.987T=	NP_001272329.1:p.Pro329=
NM_001285401.3:c.981T=	NP_001272330.1:p.Pro327=
NM_001285402.2:c.936T=	NP_001272331.1:p.Pro312=
NM_001285403.3:c.*1024T=	NP_001272332.1:n.*1024T=
NM_014336.5:c.1053T= MANE Select	NP_055151.3:p.Pro351=
NM_001285403.4:c.*1024T=	NP_001272332.1:n.*1024T=