Canonical Allele Identifier: CA497687295
Gene: AIPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6328825T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425505T>G , CM000679.2:g.6425505T>G GRCh38
NC_000017.10:g.6328825T>G , CM000679.1:g.6328825T>G GRCh37
NC_000017.9:g.6269549T>G NCBI36
NG_008474.1:g.14695A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.1110A>C MANE Select ENSP00000370521.3:p.Pro370=
ENST00000250087.9:c.921A>C ENSP00000250087.5:p.Pro307=
ENST00000381128.2:c.*982A>C ENSP00000370520.2:n.*982A>C
ENST00000381129.7:c.1110A>C ENSP00000370521.3:p.Pro370=
ENST00000570466.5:c.1044A>C ENSP00000461287.1:p.Pro348=
ENST00000570584.5:c.251+8414A>C
ENST00000574506.5:c.1074A>C ENSP00000458456.1:p.Pro358=
ENST00000575265.5:c.*1081A>C ENSP00000459673.1:n.*1081A>C
ENST00000576307.5:c.930A>C ENSP00000459522.1:p.Pro310=
ENST00000576776.5:c.1038A>C ENSP00000460827.1:p.Pro346=
ENST00000621374.4:c.*128A>C ENSP00000481337.1:n.*128A>C
NM_001033054.2:c.921A>C NP_001028226.1:p.Pro307=
NM_001033055.2:c.930A>C NP_001028227.1:p.Pro310=
NM_001285399.2:c.1074A>C NP_001272328.1:p.Pro358=
NM_001285400.2:c.1044A>C NP_001272329.1:p.Pro348=
NM_001285401.2:c.1038A>C NP_001272330.1:p.Pro346=
NM_001285402.1:c.993A>C NP_001272331.1:p.Pro331=
NM_014336.4:c.1110A>C NP_055151.3:p.Pro370=
NM_001033054.3:c.921A>C NP_001028226.1:p.Pro307=
NM_001033055.3:c.930A>C NP_001028227.1:p.Pro310=
NM_001285399.3:c.1074A>C NP_001272328.1:p.Pro358=
NM_001285400.3:c.1044A>C NP_001272329.1:p.Pro348=
NM_001285401.3:c.1038A>C NP_001272330.1:p.Pro346=
NM_001285402.2:c.993A>C NP_001272331.1:p.Pro331=
NM_001285403.3:c.*1081A>C NP_001272332.1:n.*1081A>C
NM_014336.5:c.1110A>C MANE Select NP_055151.3:p.Pro370=
NM_001285403.4:c.*1081A>C NP_001272332.1:n.*1081A>C