Canonical Allele Identifier: CA397394542

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6328973A>G (hg19) ; chr17:g.6425653A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425653A>G , CM000679.2:g.6425653A>G	GRCh38
NC_000017.10:g.6328973A>G , CM000679.1:g.6328973A>G	GRCh37
NC_000017.9:g.6269697A>G	NCBI36
NG_008474.1:g.14547T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.962T>C MANE Select	ENSP00000370521.3:p.Leu321Pro
ENST00000250087.9:c.773T>C	ENSP00000250087.5:p.Leu258Pro
ENST00000381128.2:c.*834T>C	ENSP00000370520.2:n.*834T>C
ENST00000381129.7:c.962T>C	ENSP00000370521.3:p.Leu321Pro
ENST00000570466.5:c.896T>C	ENSP00000461287.1:p.Leu299Pro
ENST00000570584.5:c.251+8266T>C
ENST00000574506.5:c.926T>C	ENSP00000458456.1:p.Leu309Pro
ENST00000575265.5:c.*933T>C	ENSP00000459673.1:n.*933T>C
ENST00000576307.5:c.782T>C	ENSP00000459522.1:p.Leu261Pro
ENST00000576776.5:c.890T>C	ENSP00000460827.1:p.Leu297Pro
ENST00000621374.4:c.961T>C	ENSP00000481337.1:p.Cys321Arg
NM_001033054.2:c.773T>C	NP_001028226.1:p.Leu258Pro
NM_001033055.2:c.782T>C	NP_001028227.1:p.Leu261Pro
NM_001285399.2:c.926T>C	NP_001272328.1:p.Leu309Pro
NM_001285400.2:c.896T>C	NP_001272329.1:p.Leu299Pro
NM_001285401.2:c.890T>C	NP_001272330.1:p.Leu297Pro
NM_001285402.1:c.845T>C	NP_001272331.1:p.Leu282Pro
NM_014336.4:c.962T>C	NP_055151.3:p.Leu321Pro
NM_001033054.3:c.773T>C	NP_001028226.1:p.Leu258Pro
NM_001033055.3:c.782T>C	NP_001028227.1:p.Leu261Pro
NM_001285399.3:c.926T>C	NP_001272328.1:p.Leu309Pro
NM_001285400.3:c.896T>C	NP_001272329.1:p.Leu299Pro
NM_001285401.3:c.890T>C	NP_001272330.1:p.Leu297Pro
NM_001285402.2:c.845T>C	NP_001272331.1:p.Leu282Pro
NM_001285403.3:c.*933T>C	NP_001272332.1:n.*933T>C
NM_014336.5:c.962T>C MANE Select	NP_055151.3:p.Leu321Pro
NM_001285403.4:c.*933T>C	NP_001272332.1:n.*933T>C