Canonical Allele Identifier: CA497687357
Gene: AIPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6328897T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425577T>C , CM000679.2:g.6425577T>C GRCh38
NC_000017.10:g.6328897T>C , CM000679.1:g.6328897T>C GRCh37
NC_000017.9:g.6269621T>C NCBI36
NG_008474.1:g.14623A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1038A>G MANE Select ENSP00000370521.3:p.Ser346=
ENST00000250087.9:c.849A>G ENSP00000250087.5:p.Ser283=
ENST00000381128.2:c.*910A>G ENSP00000370520.2:n.*910A>G
ENST00000381129.7:c.1038A>G ENSP00000370521.3:p.Ser346=
ENST00000570466.5:c.972A>G ENSP00000461287.1:p.Ser324=
ENST00000570584.5:c.251+8342A>G
ENST00000574506.5:c.1002A>G ENSP00000458456.1:p.Ser334=
ENST00000575265.5:c.*1009A>G ENSP00000459673.1:n.*1009A>G
ENST00000576307.5:c.858A>G ENSP00000459522.1:p.Ser286=
ENST00000576776.5:c.966A>G ENSP00000460827.1:p.Ser322=
ENST00000621374.4:c.*56A>G ENSP00000481337.1:n.*56A>G
NM_001033054.2:c.849A>G NP_001028226.1:p.Ser283=
NM_001033055.2:c.858A>G NP_001028227.1:p.Ser286=
NM_001285399.2:c.1002A>G NP_001272328.1:p.Ser334=
NM_001285400.2:c.972A>G NP_001272329.1:p.Ser324=
NM_001285401.2:c.966A>G NP_001272330.1:p.Ser322=
NM_001285402.1:c.921A>G NP_001272331.1:p.Ser307=
NM_014336.4:c.1038A>G NP_055151.3:p.Ser346=
NM_001033054.3:c.849A>G NP_001028226.1:p.Ser283=
NM_001033055.3:c.858A>G NP_001028227.1:p.Ser286=
NM_001285399.3:c.1002A>G NP_001272328.1:p.Ser334=
NM_001285400.3:c.972A>G NP_001272329.1:p.Ser324=
NM_001285401.3:c.966A>G NP_001272330.1:p.Ser322=
NM_001285402.2:c.921A>G NP_001272331.1:p.Ser307=
NM_001285403.3:c.*1009A>G NP_001272332.1:n.*1009A>G
NM_014336.5:c.1038A>G MANE Select NP_055151.3:p.Ser346=
NM_001285403.4:c.*1009A>G NP_001272332.1:n.*1009A>G