Canonical Allele Identifier: CA656318000

Gene: AIPL1

Linked Data

• COSMIC: COSN15660776

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425407_6425408insC , CM000679.2:g.6425407_6425408insC	GRCh38
NC_000017.10:g.6328727_6328728insC , CM000679.1:g.6328727_6328728insC	GRCh37
NC_000017.9:g.6269451_6269452insC	NCBI36
NG_008474.1:g.14792_14793insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.*52_*53insG MANE Select	ENSP00000370521.3:n.*52_*53insG
ENST00000250087.9:c.*52_*53insG	ENSP00000250087.5:n.*52_*53insG
ENST00000381128.2:c.*1079_*1080insG	ENSP00000370520.2:n.*1079_*1080insG
ENST00000381129.7:c.*52_*53insG	ENSP00000370521.3:n.*52_*53insG
ENST00000570466.5:c.*52_*53insG	ENSP00000461287.1:n.*52_*53insG
ENST00000570584.5:c.251+8511_251+8512insG
ENST00000574506.5:c.*52_*53insG	ENSP00000458456.1:n.*52_*53insG
ENST00000575265.5:c.*1178_*1179insG	ENSP00000459673.1:n.*1178_*1179insG
ENST00000576307.5:c.*52_*53insG	ENSP00000459522.1:n.*52_*53insG
ENST00000576776.5:c.*52_*53insG	ENSP00000460827.1:n.*52_*53insG
ENST00000621374.4:c.*225_*226insG	ENSP00000481337.1:n.*225_*226insG
NM_001033054.2:c.*52_*53insG	NP_001028226.1:n.*52_*53insG
NM_001033055.2:c.*52_*53insG	NP_001028227.1:n.*52_*53insG
NM_001285399.2:c.*52_*53insG	NP_001272328.1:n.*52_*53insG
NM_001285400.2:c.*52_*53insG	NP_001272329.1:n.*52_*53insG
NM_001285401.2:c.*52_*53insG	NP_001272330.1:n.*52_*53insG
NM_001285402.1:c.*52_*53insG	NP_001272331.1:n.*52_*53insG
NM_014336.4:c.*52_*53insG	NP_055151.3:n.*52_*53insG
NM_001033054.3:c.*52_*53insG	NP_001028226.1:n.*52_*53insG
NM_001033055.3:c.*52_*53insG	NP_001028227.1:n.*52_*53insG
NM_001285399.3:c.*52_*53insG	NP_001272328.1:n.*52_*53insG
NM_001285400.3:c.*52_*53insG	NP_001272329.1:n.*52_*53insG
NM_001285401.3:c.*52_*53insG	NP_001272330.1:n.*52_*53insG
NM_001285402.2:c.*52_*53insG	NP_001272331.1:n.*52_*53insG
NM_001285403.3:c.*1178_*1179insG	NP_001272332.1:n.*1178_*1179insG
NM_014336.5:c.*52_*53insG MANE Select	NP_055151.3:n.*52_*53insG
NM_001285403.4:c.*1178_*1179insG	NP_001272332.1:n.*1178_*1179insG