Canonical Allele Identifier: CA397394382

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6328896A>T (hg19) ; chr17:g.6425576A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425576A>T , CM000679.2:g.6425576A>T	GRCh38
NC_000017.10:g.6328896A>T , CM000679.1:g.6328896A>T	GRCh37
NC_000017.9:g.6269620A>T	NCBI36
NG_008474.1:g.14624T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1039T>A MANE Select	ENSP00000370521.3:p.Ser347Thr
ENST00000250087.9:c.850T>A	ENSP00000250087.5:p.Ser284Thr
ENST00000381128.2:c.*911T>A	ENSP00000370520.2:n.*911T>A
ENST00000381129.7:c.1039T>A	ENSP00000370521.3:p.Ser347Thr
ENST00000570466.5:c.973T>A	ENSP00000461287.1:p.Ser325Thr
ENST00000570584.5:c.251+8343T>A
ENST00000574506.5:c.1003T>A	ENSP00000458456.1:p.Ser335Thr
ENST00000575265.5:c.*1010T>A	ENSP00000459673.1:n.*1010T>A
ENST00000576307.5:c.859T>A	ENSP00000459522.1:p.Ser287Thr
ENST00000576776.5:c.967T>A	ENSP00000460827.1:p.Ser323Thr
ENST00000621374.4:c.*57T>A	ENSP00000481337.1:n.*57T>A
NM_001033054.2:c.850T>A	NP_001028226.1:p.Ser284Thr
NM_001033055.2:c.859T>A	NP_001028227.1:p.Ser287Thr
NM_001285399.2:c.1003T>A	NP_001272328.1:p.Ser335Thr
NM_001285400.2:c.973T>A	NP_001272329.1:p.Ser325Thr
NM_001285401.2:c.967T>A	NP_001272330.1:p.Ser323Thr
NM_001285402.1:c.922T>A	NP_001272331.1:p.Ser308Thr
NM_014336.4:c.1039T>A	NP_055151.3:p.Ser347Thr
NM_001033054.3:c.850T>A	NP_001028226.1:p.Ser284Thr
NM_001033055.3:c.859T>A	NP_001028227.1:p.Ser287Thr
NM_001285399.3:c.1003T>A	NP_001272328.1:p.Ser335Thr
NM_001285400.3:c.973T>A	NP_001272329.1:p.Ser325Thr
NM_001285401.3:c.967T>A	NP_001272330.1:p.Ser323Thr
NM_001285402.2:c.922T>A	NP_001272331.1:p.Ser308Thr
NM_001285403.3:c.*1010T>A	NP_001272332.1:n.*1010T>A
NM_014336.5:c.1039T>A MANE Select	NP_055151.3:p.Ser347Thr
NM_001285403.4:c.*1010T>A	NP_001272332.1:n.*1010T>A