Canonical Allele Identifier: CA397394333

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6328872G>T (hg19) ; chr17:g.6425552G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425552G>T , CM000679.2:g.6425552G>T	GRCh38
NC_000017.10:g.6328872G>T , CM000679.1:g.6328872G>T	GRCh37
NC_000017.9:g.6269596G>T	NCBI36
NG_008474.1:g.14648C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.1063C>A MANE Select	ENSP00000370521.3:p.Pro355Thr
ENST00000250087.9:c.874C>A	ENSP00000250087.5:p.Pro292Thr
ENST00000381128.2:c.*935C>A	ENSP00000370520.2:n.*935C>A
ENST00000381129.7:c.1063C>A	ENSP00000370521.3:p.Pro355Thr
ENST00000570466.5:c.997C>A	ENSP00000461287.1:p.Pro333Thr
ENST00000570584.5:c.251+8367C>A
ENST00000574506.5:c.1027C>A	ENSP00000458456.1:p.Pro343Thr
ENST00000575265.5:c.*1034C>A	ENSP00000459673.1:n.*1034C>A
ENST00000576307.5:c.883C>A	ENSP00000459522.1:p.Pro295Thr
ENST00000576776.5:c.991C>A	ENSP00000460827.1:p.Pro331Thr
ENST00000621374.4:c.*81C>A	ENSP00000481337.1:n.*81C>A
NM_001033054.2:c.874C>A	NP_001028226.1:p.Pro292Thr
NM_001033055.2:c.883C>A	NP_001028227.1:p.Pro295Thr
NM_001285399.2:c.1027C>A	NP_001272328.1:p.Pro343Thr
NM_001285400.2:c.997C>A	NP_001272329.1:p.Pro333Thr
NM_001285401.2:c.991C>A	NP_001272330.1:p.Pro331Thr
NM_001285402.1:c.946C>A	NP_001272331.1:p.Pro316Thr
NM_014336.4:c.1063C>A	NP_055151.3:p.Pro355Thr
NM_001033054.3:c.874C>A	NP_001028226.1:p.Pro292Thr
NM_001033055.3:c.883C>A	NP_001028227.1:p.Pro295Thr
NM_001285399.3:c.1027C>A	NP_001272328.1:p.Pro343Thr
NM_001285400.3:c.997C>A	NP_001272329.1:p.Pro333Thr
NM_001285401.3:c.991C>A	NP_001272330.1:p.Pro331Thr
NM_001285402.2:c.946C>A	NP_001272331.1:p.Pro316Thr
NM_001285403.3:c.*1034C>A	NP_001272332.1:n.*1034C>A
NM_014336.5:c.1063C>A MANE Select	NP_055151.3:p.Pro355Thr
NM_001285403.4:c.*1034C>A	NP_001272332.1:n.*1034C>A