Canonical Allele Identifier: CA397394426
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1911843702

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425599G>T , CM000679.2:g.6425599G>T GRCh38
NC_000017.10:g.6328919G>T , CM000679.1:g.6328919G>T GRCh37
NC_000017.9:g.6269643G>T NCBI36
NG_008474.1:g.14601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.1016C>A MANE Select ENSP00000370521.3:p.Pro339His
ENST00000250087.9:c.827C>A ENSP00000250087.5:p.Pro276His
ENST00000381128.2:c.*888C>A ENSP00000370520.2:n.*888C>A
ENST00000381129.7:c.1016C>A ENSP00000370521.3:p.Pro339His
ENST00000570466.5:c.950C>A ENSP00000461287.1:p.Pro317His
ENST00000570584.5:c.251+8320C>A
ENST00000574506.5:c.980C>A ENSP00000458456.1:p.Pro327His
ENST00000575265.5:c.*987C>A ENSP00000459673.1:n.*987C>A
ENST00000576307.5:c.836C>A ENSP00000459522.1:p.Pro279His
ENST00000576776.5:c.944C>A ENSP00000460827.1:p.Pro315His
ENST00000621374.4:c.*34C>A ENSP00000481337.1:n.*34C>A
NM_001033054.2:c.827C>A NP_001028226.1:p.Pro276His
NM_001033055.2:c.836C>A NP_001028227.1:p.Pro279His
NM_001285399.2:c.980C>A NP_001272328.1:p.Pro327His
NM_001285400.2:c.950C>A NP_001272329.1:p.Pro317His
NM_001285401.2:c.944C>A NP_001272330.1:p.Pro315His
NM_001285402.1:c.899C>A NP_001272331.1:p.Pro300His
NM_014336.4:c.1016C>A NP_055151.3:p.Pro339His
NM_001033054.3:c.827C>A NP_001028226.1:p.Pro276His
NM_001033055.3:c.836C>A NP_001028227.1:p.Pro279His
NM_001285399.3:c.980C>A NP_001272328.1:p.Pro327His
NM_001285400.3:c.950C>A NP_001272329.1:p.Pro317His
NM_001285401.3:c.944C>A NP_001272330.1:p.Pro315His
NM_001285402.2:c.899C>A NP_001272331.1:p.Pro300His
NM_001285403.3:c.*987C>A NP_001272332.1:n.*987C>A
NM_014336.5:c.1016C>A MANE Select NP_055151.3:p.Pro339His
NM_001285403.4:c.*987C>A NP_001272332.1:n.*987C>A