Canonical Allele Identifier: CA397394373

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6328892G>C (hg19) ; chr17:g.6425572G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425572G>C , CM000679.2:g.6425572G>C	GRCh38
NC_000017.10:g.6328892G>C , CM000679.1:g.6328892G>C	GRCh37
NC_000017.9:g.6269616G>C	NCBI36
NG_008474.1:g.14628C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.1043C>G MANE Select	ENSP00000370521.3:p.Thr348Arg
ENST00000250087.9:c.854C>G	ENSP00000250087.5:p.Thr285Arg
ENST00000381128.2:c.*915C>G	ENSP00000370520.2:n.*915C>G
ENST00000381129.7:c.1043C>G	ENSP00000370521.3:p.Thr348Arg
ENST00000570466.5:c.977C>G	ENSP00000461287.1:p.Thr326Arg
ENST00000570584.5:c.251+8347C>G
ENST00000574506.5:c.1007C>G	ENSP00000458456.1:p.Thr336Arg
ENST00000575265.5:c.*1014C>G	ENSP00000459673.1:n.*1014C>G
ENST00000576307.5:c.863C>G	ENSP00000459522.1:p.Thr288Arg
ENST00000576776.5:c.971C>G	ENSP00000460827.1:p.Thr324Arg
ENST00000621374.4:c.*61C>G	ENSP00000481337.1:n.*61C>G
NM_001033054.2:c.854C>G	NP_001028226.1:p.Thr285Arg
NM_001033055.2:c.863C>G	NP_001028227.1:p.Thr288Arg
NM_001285399.2:c.1007C>G	NP_001272328.1:p.Thr336Arg
NM_001285400.2:c.977C>G	NP_001272329.1:p.Thr326Arg
NM_001285401.2:c.971C>G	NP_001272330.1:p.Thr324Arg
NM_001285402.1:c.926C>G	NP_001272331.1:p.Thr309Arg
NM_014336.4:c.1043C>G	NP_055151.3:p.Thr348Arg
NM_001033054.3:c.854C>G	NP_001028226.1:p.Thr285Arg
NM_001033055.3:c.863C>G	NP_001028227.1:p.Thr288Arg
NM_001285399.3:c.1007C>G	NP_001272328.1:p.Thr336Arg
NM_001285400.3:c.977C>G	NP_001272329.1:p.Thr326Arg
NM_001285401.3:c.971C>G	NP_001272330.1:p.Thr324Arg
NM_001285402.2:c.926C>G	NP_001272331.1:p.Thr309Arg
NM_001285403.3:c.*1014C>G	NP_001272332.1:n.*1014C>G
NM_014336.5:c.1043C>G MANE Select	NP_055151.3:p.Thr348Arg
NM_001285403.4:c.*1014C>G	NP_001272332.1:n.*1014C>G