Canonical Allele Identifier: CA2635688699

Gene: AIPL1

Linked Data

• gnomAD v4: 17-6425309-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425309_6425310insG , CM000679.2:g.6425309_6425310insG	GRCh38
NC_000017.10:g.6328629_6328630insG , CM000679.1:g.6328629_6328630insG	GRCh37
NC_000017.9:g.6269353_6269354insG	NCBI36
NG_008474.1:g.14890_14891insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.*150_*151insC MANE Select	ENSP00000370521.3:n.*150_*151insC
ENST00000250087.9:c.*150_*151insC	ENSP00000250087.5:n.*150_*151insC
ENST00000381128.2:c.*1177_*1178insC	ENSP00000370520.2:n.*1177_*1178insC
ENST00000381129.7:c.*150_*151insC	ENSP00000370521.3:n.*150_*151insC
ENST00000570584.5:c.251+8609_251+8610insC
ENST00000574506.5:c.*150_*151insC	ENSP00000458456.1:n.*150_*151insC
ENST00000575265.5:c.*1276_*1277insC	ENSP00000459673.1:n.*1276_*1277insC
NM_001033054.2:c.*150_*151insC	NP_001028226.1:n.*150_*151insC
NM_001033055.2:c.*150_*151insC	NP_001028227.1:n.*150_*151insC
NM_001285399.2:c.*150_*151insC	NP_001272328.1:n.*150_*151insC
NM_001285400.2:c.*150_*151insC	NP_001272329.1:n.*150_*151insC
NM_001285401.2:c.*150_*151insC	NP_001272330.1:n.*150_*151insC
NM_001285402.1:c.*150_*151insC	NP_001272331.1:n.*150_*151insC
NM_014336.4:c.*150_*151insC	NP_055151.3:n.*150_*151insC
NM_001033054.3:c.*150_*151insC	NP_001028226.1:n.*150_*151insC
NM_001033055.3:c.*150_*151insC	NP_001028227.1:n.*150_*151insC
NM_001285399.3:c.*150_*151insC	NP_001272328.1:n.*150_*151insC
NM_001285400.3:c.*150_*151insC	NP_001272329.1:n.*150_*151insC
NM_001285401.3:c.*150_*151insC	NP_001272330.1:n.*150_*151insC
NM_001285402.2:c.*150_*151insC	NP_001272331.1:n.*150_*151insC
NM_001285403.3:c.*1276_*1277insC	NP_001272332.1:n.*1276_*1277insC
NM_014336.5:c.*150_*151insC MANE Select	NP_055151.3:n.*150_*151insC
NM_001285403.4:c.*1276_*1277insC	NP_001272332.1:n.*1276_*1277insC