Canonical Allele Identifier: CA397394612
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1911861988

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425679C>T , CM000679.2:g.6425679C>T GRCh38
NC_000017.10:g.6328999C>T , CM000679.1:g.6328999C>T GRCh37
NC_000017.9:g.6269723C>T NCBI36
NG_008474.1:g.14521G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381129.8:c.936G>A MANE Select ENSP00000370521.3:p.Met312Ile
ENST00000250087.9:c.747G>A ENSP00000250087.5:p.Met249Ile
ENST00000381128.2:c.*808G>A ENSP00000370520.2:n.*808G>A
ENST00000381129.7:c.936G>A ENSP00000370521.3:p.Met312Ile
ENST00000570466.5:c.870G>A ENSP00000461287.1:p.Met290Ile
ENST00000570584.5:c.251+8240G>A
ENST00000574506.5:c.900G>A ENSP00000458456.1:p.Met300Ile
ENST00000575265.5:c.*907G>A ENSP00000459673.1:n.*907G>A
ENST00000576307.5:c.756G>A ENSP00000459522.1:p.Met252Ile
ENST00000576776.5:c.864G>A ENSP00000460827.1:p.Met288Ile
ENST00000621374.4:c.935G>A ENSP00000481337.1:p.Trp312Ter
NM_001033054.2:c.747G>A NP_001028226.1:p.Met249Ile
NM_001033055.2:c.756G>A NP_001028227.1:p.Met252Ile
NM_001285399.2:c.900G>A NP_001272328.1:p.Met300Ile
NM_001285400.2:c.870G>A NP_001272329.1:p.Met290Ile
NM_001285401.2:c.864G>A NP_001272330.1:p.Met288Ile
NM_001285402.1:c.819G>A NP_001272331.1:p.Met273Ile
NM_014336.4:c.936G>A NP_055151.3:p.Met312Ile
NM_001033054.3:c.747G>A NP_001028226.1:p.Met249Ile
NM_001033055.3:c.756G>A NP_001028227.1:p.Met252Ile
NM_001285399.3:c.900G>A NP_001272328.1:p.Met300Ile
NM_001285400.3:c.870G>A NP_001272329.1:p.Met290Ile
NM_001285401.3:c.864G>A NP_001272330.1:p.Met288Ile
NM_001285402.2:c.819G>A NP_001272331.1:p.Met273Ile
NM_001285403.3:c.*907G>A NP_001272332.1:n.*907G>A
NM_014336.5:c.936G>A MANE Select NP_055151.3:p.Met312Ile
NM_001285403.4:c.*907G>A NP_001272332.1:n.*907G>A