Canonical Allele Identifier: CA2635688630

Gene: AIPL1

Linked Data

• gnomAD v4: 17-6425261-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425261G>A , CM000679.2:g.6425261G>A	GRCh38
NC_000017.10:g.6328581G>A , CM000679.1:g.6328581G>A	GRCh37
NC_000017.9:g.6269305G>A	NCBI36
NG_008474.1:g.14939C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.*199C>T MANE Select	ENSP00000370521.3:n.*199C>T
ENST00000250087.9:c.*199C>T	ENSP00000250087.5:n.*199C>T
ENST00000381128.2:c.*1226C>T	ENSP00000370520.2:n.*1226C>T
ENST00000381129.7:c.*199C>T	ENSP00000370521.3:n.*199C>T
ENST00000570584.5:c.251+8658C>T
ENST00000574506.5:c.*199C>T	ENSP00000458456.1:n.*199C>T
NM_001033054.2:c.*199C>T	NP_001028226.1:n.*199C>T
NM_001033055.2:c.*199C>T	NP_001028227.1:n.*199C>T
NM_001285399.2:c.*199C>T	NP_001272328.1:n.*199C>T
NM_001285400.2:c.*199C>T	NP_001272329.1:n.*199C>T
NM_001285401.2:c.*199C>T	NP_001272330.1:n.*199C>T
NM_001285402.1:c.*199C>T	NP_001272331.1:n.*199C>T
NM_014336.4:c.*199C>T	NP_055151.3:n.*199C>T
NM_001033054.3:c.*199C>T	NP_001028226.1:n.*199C>T
NM_001033055.3:c.*199C>T	NP_001028227.1:n.*199C>T
NM_001285399.3:c.*199C>T	NP_001272328.1:n.*199C>T
NM_001285400.3:c.*199C>T	NP_001272329.1:n.*199C>T
NM_001285401.3:c.*199C>T	NP_001272330.1:n.*199C>T
NM_001285402.2:c.*199C>T	NP_001272331.1:n.*199C>T
NM_014336.5:c.*199C>T MANE Select	NP_055151.3:n.*199C>T
NM_001285403.4:c.*1325C>T	NP_001272332.1:n.*1325C>T