Canonical Allele Identifier: CA397394634
Gene: AIPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425687T>A , CM000679.2:g.6425687T>A GRCh38
NC_000017.10:g.6329007T>A , CM000679.1:g.6329007T>A GRCh37
NC_000017.9:g.6269731T>A NCBI36
NG_008474.1:g.14513A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.928A>T MANE Select ENSP00000370521.3:p.Asn310Tyr
ENST00000250087.9:c.739A>T ENSP00000250087.5:p.Asn247Tyr
ENST00000381128.2:c.*800A>T ENSP00000370520.2:n.*800A>T
ENST00000381129.7:c.928A>T ENSP00000370521.3:p.Asn310Tyr
ENST00000570466.5:c.862A>T ENSP00000461287.1:p.Asn288Tyr
ENST00000570584.5:c.251+8232A>T
ENST00000574506.5:c.892A>T ENSP00000458456.1:p.Asn298Tyr
ENST00000575265.5:c.*899A>T ENSP00000459673.1:n.*899A>T
ENST00000576307.5:c.748A>T ENSP00000459522.1:p.Asn250Tyr
ENST00000576776.5:c.856A>T ENSP00000460827.1:p.Asn286Tyr
ENST00000621374.4:c.928A>T ENSP00000481337.1:p.Asn310Tyr
NM_001033054.2:c.739A>T NP_001028226.1:p.Asn247Tyr
NM_001033055.2:c.748A>T NP_001028227.1:p.Asn250Tyr
NM_001285399.2:c.892A>T NP_001272328.1:p.Asn298Tyr
NM_001285400.2:c.862A>T NP_001272329.1:p.Asn288Tyr
NM_001285401.2:c.856A>T NP_001272330.1:p.Asn286Tyr
NM_001285402.1:c.811A>T NP_001272331.1:p.Asn271Tyr
NM_014336.4:c.928A>T NP_055151.3:p.Asn310Tyr
NM_001033054.3:c.739A>T NP_001028226.1:p.Asn247Tyr
NM_001033055.3:c.748A>T NP_001028227.1:p.Asn250Tyr
NM_001285399.3:c.892A>T NP_001272328.1:p.Asn298Tyr
NM_001285400.3:c.862A>T NP_001272329.1:p.Asn288Tyr
NM_001285401.3:c.856A>T NP_001272330.1:p.Asn286Tyr
NM_001285402.2:c.811A>T NP_001272331.1:p.Asn271Tyr
NM_001285403.3:c.*899A>T NP_001272332.1:n.*899A>T
NM_014336.5:c.928A>T MANE Select NP_055151.3:p.Asn310Tyr
NM_001285403.4:c.*899A>T NP_001272332.1:n.*899A>T