Canonical Allele Identifier: CA397394259

Gene: AIPL1

Linked Data

• dbSNP Id: rs1196546609
• gnomAD v2: 17-6328832-G-T
• gnomAD v4: 17-6425512-G-T
• MyVariant Identifiers: chr17:g.6328832G>T (hg19) ; chr17:g.6425512G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425512G>T , CM000679.2:g.6425512G>T	GRCh38
NC_000017.10:g.6328832G>T , CM000679.1:g.6328832G>T	GRCh37
NC_000017.9:g.6269556G>T	NCBI36
NG_008474.1:g.14688C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.1103C>A MANE Select	ENSP00000370521.3:p.Ala368Glu
ENST00000250087.9:c.914C>A	ENSP00000250087.5:p.Ala305Glu
ENST00000381128.2:c.*975C>A	ENSP00000370520.2:n.*975C>A
ENST00000381129.7:c.1103C>A	ENSP00000370521.3:p.Ala368Glu
ENST00000570466.5:c.1037C>A	ENSP00000461287.1:p.Ala346Glu
ENST00000570584.5:c.251+8407C>A
ENST00000574506.5:c.1067C>A	ENSP00000458456.1:p.Ala356Glu
ENST00000575265.5:c.*1074C>A	ENSP00000459673.1:n.*1074C>A
ENST00000576307.5:c.923C>A	ENSP00000459522.1:p.Ala308Glu
ENST00000576776.5:c.1031C>A	ENSP00000460827.1:p.Ala344Glu
ENST00000621374.4:c.*121C>A	ENSP00000481337.1:n.*121C>A
NM_001033054.2:c.914C>A	NP_001028226.1:p.Ala305Glu
NM_001033055.2:c.923C>A	NP_001028227.1:p.Ala308Glu
NM_001285399.2:c.1067C>A	NP_001272328.1:p.Ala356Glu
NM_001285400.2:c.1037C>A	NP_001272329.1:p.Ala346Glu
NM_001285401.2:c.1031C>A	NP_001272330.1:p.Ala344Glu
NM_001285402.1:c.986C>A	NP_001272331.1:p.Ala329Glu
NM_014336.4:c.1103C>A	NP_055151.3:p.Ala368Glu
NM_001033054.3:c.914C>A	NP_001028226.1:p.Ala305Glu
NM_001033055.3:c.923C>A	NP_001028227.1:p.Ala308Glu
NM_001285399.3:c.1067C>A	NP_001272328.1:p.Ala356Glu
NM_001285400.3:c.1037C>A	NP_001272329.1:p.Ala346Glu
NM_001285401.3:c.1031C>A	NP_001272330.1:p.Ala344Glu
NM_001285402.2:c.986C>A	NP_001272331.1:p.Ala329Glu
NM_001285403.3:c.*1074C>A	NP_001272332.1:n.*1074C>A
NM_014336.5:c.1103C>A MANE Select	NP_055151.3:p.Ala368Glu
NM_001285403.4:c.*1074C>A	NP_001272332.1:n.*1074C>A