Canonical Allele Identifier: CA397394442

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6328928G>A (hg19) ; chr17:g.6425608G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425608G>A , CM000679.2:g.6425608G>A	GRCh38
NC_000017.10:g.6328928G>A , CM000679.1:g.6328928G>A	GRCh37
NC_000017.9:g.6269652G>A	NCBI36
NG_008474.1:g.14592C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.1007C>T MANE Select	ENSP00000370521.3:p.Ala336Val
ENST00000250087.9:c.818C>T	ENSP00000250087.5:p.Ala273Val
ENST00000381128.2:c.*879C>T	ENSP00000370520.2:n.*879C>T
ENST00000381129.7:c.1007C>T	ENSP00000370521.3:p.Ala336Val
ENST00000570466.5:c.941C>T	ENSP00000461287.1:p.Ala314Val
ENST00000570584.5:c.251+8311C>T
ENST00000574506.5:c.971C>T	ENSP00000458456.1:p.Ala324Val
ENST00000575265.5:c.*978C>T	ENSP00000459673.1:n.*978C>T
ENST00000576307.5:c.827C>T	ENSP00000459522.1:p.Ala276Val
ENST00000576776.5:c.935C>T	ENSP00000460827.1:p.Ala312Val
ENST00000621374.4:c.*25C>T	ENSP00000481337.1:n.*25C>T
NM_001033054.2:c.818C>T	NP_001028226.1:p.Ala273Val
NM_001033055.2:c.827C>T	NP_001028227.1:p.Ala276Val
NM_001285399.2:c.971C>T	NP_001272328.1:p.Ala324Val
NM_001285400.2:c.941C>T	NP_001272329.1:p.Ala314Val
NM_001285401.2:c.935C>T	NP_001272330.1:p.Ala312Val
NM_001285402.1:c.890C>T	NP_001272331.1:p.Ala297Val
NM_014336.4:c.1007C>T	NP_055151.3:p.Ala336Val
NM_001033054.3:c.818C>T	NP_001028226.1:p.Ala273Val
NM_001033055.3:c.827C>T	NP_001028227.1:p.Ala276Val
NM_001285399.3:c.971C>T	NP_001272328.1:p.Ala324Val
NM_001285400.3:c.941C>T	NP_001272329.1:p.Ala314Val
NM_001285401.3:c.935C>T	NP_001272330.1:p.Ala312Val
NM_001285402.2:c.890C>T	NP_001272331.1:p.Ala297Val
NM_001285403.3:c.*978C>T	NP_001272332.1:n.*978C>T
NM_014336.5:c.1007C>T MANE Select	NP_055151.3:p.Ala336Val
NM_001285403.4:c.*978C>T	NP_001272332.1:n.*978C>T