Canonical Allele Identifier: CA2245346489

Gene: AIPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425472C= , CM000679.2:g.6425472C=	GRCh38
NC_000017.10:g.6328792C= , CM000679.1:g.6328792C=	GRCh37
NC_000017.9:g.6269516C=	NCBI36
NG_008474.1:g.14728G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1143G= MANE Select	ENSP00000370521.3:p.Ser381=
ENST00000250087.9:c.954G=	ENSP00000250087.5:p.Ser318=
ENST00000381128.2:c.*1015G=	ENSP00000370520.2:n.*1015G=
ENST00000381129.7:c.1143G=	ENSP00000370521.3:p.Ser381=
ENST00000570466.5:c.1077G=	ENSP00000461287.1:p.Ser359=
ENST00000570584.5:c.251+8447G=
ENST00000574506.5:c.1107G=	ENSP00000458456.1:p.Ser369=
ENST00000575265.5:c.*1114G=	ENSP00000459673.1:n.*1114G=
ENST00000576307.5:c.963G=	ENSP00000459522.1:p.Ser321=
ENST00000576776.5:c.1071G=	ENSP00000460827.1:p.Ser357=
ENST00000621374.4:c.*161G=	ENSP00000481337.1:n.*161G=
NM_001033054.2:c.954G=	NP_001028226.1:p.Ser318=
NM_001033055.2:c.963G=	NP_001028227.1:p.Ser321=
NM_001285399.2:c.1107G=	NP_001272328.1:p.Ser369=
NM_001285400.2:c.1077G=	NP_001272329.1:p.Ser359=
NM_001285401.2:c.1071G=	NP_001272330.1:p.Ser357=
NM_001285402.1:c.1026G=	NP_001272331.1:p.Ser342=
NM_014336.4:c.1143G=	NP_055151.3:p.Ser381=
NM_001033054.3:c.954G=	NP_001028226.1:p.Ser318=
NM_001033055.3:c.963G=	NP_001028227.1:p.Ser321=
NM_001285399.3:c.1107G=	NP_001272328.1:p.Ser369=
NM_001285400.3:c.1077G=	NP_001272329.1:p.Ser359=
NM_001285401.3:c.1071G=	NP_001272330.1:p.Ser357=
NM_001285402.2:c.1026G=	NP_001272331.1:p.Ser342=
NM_001285403.3:c.*1114G=	NP_001272332.1:n.*1114G=
NM_014336.5:c.1143G= MANE Select	NP_055151.3:p.Ser381=
NM_001285403.4:c.*1114G=	NP_001272332.1:n.*1114G=