Canonical Allele Identifier: CA656317991

Gene: AIPL1

Linked Data

• gnomAD v4: 17-6425314-T-TG
• COSMIC: COSN22086809

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425314_6425315insG , CM000679.2:g.6425314_6425315insG	GRCh38
NC_000017.10:g.6328634_6328635insG , CM000679.1:g.6328634_6328635insG	GRCh37
NC_000017.9:g.6269358_6269359insG	NCBI36
NG_008474.1:g.14885_14886insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.*145_*146insC MANE Select	ENSP00000370521.3:n.*145_*146insC
ENST00000250087.9:c.*145_*146insC	ENSP00000250087.5:n.*145_*146insC
ENST00000381128.2:c.*1172_*1173insC	ENSP00000370520.2:n.*1172_*1173insC
ENST00000381129.7:c.*145_*146insC	ENSP00000370521.3:n.*145_*146insC
ENST00000570584.5:c.251+8604_251+8605insC
ENST00000574506.5:c.*145_*146insC	ENSP00000458456.1:n.*145_*146insC
ENST00000575265.5:c.*1271_*1272insC	ENSP00000459673.1:n.*1271_*1272insC
NM_001033054.2:c.*145_*146insC	NP_001028226.1:n.*145_*146insC
NM_001033055.2:c.*145_*146insC	NP_001028227.1:n.*145_*146insC
NM_001285399.2:c.*145_*146insC	NP_001272328.1:n.*145_*146insC
NM_001285400.2:c.*145_*146insC	NP_001272329.1:n.*145_*146insC
NM_001285401.2:c.*145_*146insC	NP_001272330.1:n.*145_*146insC
NM_001285402.1:c.*145_*146insC	NP_001272331.1:n.*145_*146insC
NM_014336.4:c.*145_*146insC	NP_055151.3:n.*145_*146insC
NM_001033054.3:c.*145_*146insC	NP_001028226.1:n.*145_*146insC
NM_001033055.3:c.*145_*146insC	NP_001028227.1:n.*145_*146insC
NM_001285399.3:c.*145_*146insC	NP_001272328.1:n.*145_*146insC
NM_001285400.3:c.*145_*146insC	NP_001272329.1:n.*145_*146insC
NM_001285401.3:c.*145_*146insC	NP_001272330.1:n.*145_*146insC
NM_001285402.2:c.*145_*146insC	NP_001272331.1:n.*145_*146insC
NM_001285403.3:c.*1271_*1272insC	NP_001272332.1:n.*1271_*1272insC
NM_014336.5:c.*145_*146insC MANE Select	NP_055151.3:n.*145_*146insC
NM_001285403.4:c.*1271_*1272insC	NP_001272332.1:n.*1271_*1272insC