Canonical Allele Identifier: CA397394602

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6328994T>G (hg19) ; chr17:g.6425674T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425674T>G , CM000679.2:g.6425674T>G	GRCh38
NC_000017.10:g.6328994T>G , CM000679.1:g.6328994T>G	GRCh37
NC_000017.9:g.6269718T>G	NCBI36
NG_008474.1:g.14526A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.941A>C MANE Select	ENSP00000370521.3:p.Glu314Ala
ENST00000250087.9:c.752A>C	ENSP00000250087.5:p.Glu251Ala
ENST00000381128.2:c.*813A>C	ENSP00000370520.2:n.*813A>C
ENST00000381129.7:c.941A>C	ENSP00000370521.3:p.Glu314Ala
ENST00000570466.5:c.875A>C	ENSP00000461287.1:p.Glu292Ala
ENST00000570584.5:c.251+8245A>C
ENST00000574506.5:c.905A>C	ENSP00000458456.1:p.Glu302Ala
ENST00000575265.5:c.*912A>C	ENSP00000459673.1:n.*912A>C
ENST00000576307.5:c.761A>C	ENSP00000459522.1:p.Glu254Ala
ENST00000576776.5:c.869A>C	ENSP00000460827.1:p.Glu290Ala
ENST00000621374.4:c.940A>C	ENSP00000481337.1:p.Arg314=
NM_001033054.2:c.752A>C	NP_001028226.1:p.Glu251Ala
NM_001033055.2:c.761A>C	NP_001028227.1:p.Glu254Ala
NM_001285399.2:c.905A>C	NP_001272328.1:p.Glu302Ala
NM_001285400.2:c.875A>C	NP_001272329.1:p.Glu292Ala
NM_001285401.2:c.869A>C	NP_001272330.1:p.Glu290Ala
NM_001285402.1:c.824A>C	NP_001272331.1:p.Glu275Ala
NM_014336.4:c.941A>C	NP_055151.3:p.Glu314Ala
NM_001033054.3:c.752A>C	NP_001028226.1:p.Glu251Ala
NM_001033055.3:c.761A>C	NP_001028227.1:p.Glu254Ala
NM_001285399.3:c.905A>C	NP_001272328.1:p.Glu302Ala
NM_001285400.3:c.875A>C	NP_001272329.1:p.Glu292Ala
NM_001285401.3:c.869A>C	NP_001272330.1:p.Glu290Ala
NM_001285402.2:c.824A>C	NP_001272331.1:p.Glu275Ala
NM_001285403.3:c.*912A>C	NP_001272332.1:n.*912A>C
NM_014336.5:c.941A>C MANE Select	NP_055151.3:p.Glu314Ala
NM_001285403.4:c.*912A>C	NP_001272332.1:n.*912A>C