Canonical Allele Identifier: CA397394463
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1390882721
gnomAD v2: 17-6328938-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425618G>A , CM000679.2:g.6425618G>A GRCh38
NC_000017.10:g.6328938G>A , CM000679.1:g.6328938G>A GRCh37
NC_000017.9:g.6269662G>A NCBI36
NG_008474.1:g.14582C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.997C>T MANE Select ENSP00000370521.3:p.Gln333Ter
ENST00000250087.9:c.808C>T ENSP00000250087.5:p.Gln270Ter
ENST00000381128.2:c.*869C>T ENSP00000370520.2:n.*869C>T
ENST00000381129.7:c.997C>T ENSP00000370521.3:p.Gln333Ter
ENST00000570466.5:c.931C>T ENSP00000461287.1:p.Gln311Ter
ENST00000570584.5:c.251+8301C>T
ENST00000574506.5:c.961C>T ENSP00000458456.1:p.Gln321Ter
ENST00000575265.5:c.*968C>T ENSP00000459673.1:n.*968C>T
ENST00000576307.5:c.817C>T ENSP00000459522.1:p.Gln273Ter
ENST00000576776.5:c.925C>T ENSP00000460827.1:p.Gln309Ter
ENST00000621374.4:c.*15C>T ENSP00000481337.1:n.*15C>T
NM_001033054.2:c.808C>T NP_001028226.1:p.Gln270Ter
NM_001033055.2:c.817C>T NP_001028227.1:p.Gln273Ter
NM_001285399.2:c.961C>T NP_001272328.1:p.Gln321Ter
NM_001285400.2:c.931C>T NP_001272329.1:p.Gln311Ter
NM_001285401.2:c.925C>T NP_001272330.1:p.Gln309Ter
NM_001285402.1:c.880C>T NP_001272331.1:p.Gln294Ter
NM_014336.4:c.997C>T NP_055151.3:p.Gln333Ter
NM_001033054.3:c.808C>T NP_001028226.1:p.Gln270Ter
NM_001033055.3:c.817C>T NP_001028227.1:p.Gln273Ter
NM_001285399.3:c.961C>T NP_001272328.1:p.Gln321Ter
NM_001285400.3:c.931C>T NP_001272329.1:p.Gln311Ter
NM_001285401.3:c.925C>T NP_001272330.1:p.Gln309Ter
NM_001285402.2:c.880C>T NP_001272331.1:p.Gln294Ter
NM_001285403.3:c.*968C>T NP_001272332.1:n.*968C>T
NM_014336.5:c.997C>T MANE Select NP_055151.3:p.Gln333Ter
NM_001285403.4:c.*968C>T NP_001272332.1:n.*968C>T