Canonical Allele Identifier: CA2635688611

Gene: AIPL1

Linked Data

• gnomAD v4: 17-6425247-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425247A>C , CM000679.2:g.6425247A>C	GRCh38
NC_000017.10:g.6328567A>C , CM000679.1:g.6328567A>C	GRCh37
NC_000017.9:g.6269291A>C	NCBI36
NG_008474.1:g.14953T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.*213T>G MANE Select	ENSP00000370521.3:n.*213T>G
ENST00000250087.9:c.*213T>G	ENSP00000250087.5:n.*213T>G
ENST00000381128.2:c.*1240T>G	ENSP00000370520.2:n.*1240T>G
ENST00000381129.7:c.*213T>G	ENSP00000370521.3:n.*213T>G
ENST00000570584.5:c.251+8672T>G
ENST00000574506.5:c.*213T>G	ENSP00000458456.1:n.*213T>G
NM_001033054.2:c.*213T>G	NP_001028226.1:n.*213T>G
NM_001033055.2:c.*213T>G	NP_001028227.1:n.*213T>G
NM_001285399.2:c.*213T>G	NP_001272328.1:n.*213T>G
NM_001285400.2:c.*213T>G	NP_001272329.1:n.*213T>G
NM_001285401.2:c.*213T>G	NP_001272330.1:n.*213T>G
NM_001285402.1:c.*213T>G	NP_001272331.1:n.*213T>G
NM_014336.4:c.*213T>G	NP_055151.3:n.*213T>G
NM_001033054.3:c.*213T>G	NP_001028226.1:n.*213T>G
NM_001033055.3:c.*213T>G	NP_001028227.1:n.*213T>G
NM_001285399.3:c.*213T>G	NP_001272328.1:n.*213T>G
NM_001285400.3:c.*213T>G	NP_001272329.1:n.*213T>G
NM_001285401.3:c.*213T>G	NP_001272330.1:n.*213T>G
NM_001285402.2:c.*213T>G	NP_001272331.1:n.*213T>G
NM_014336.5:c.*213T>G MANE Select	NP_055151.3:n.*213T>G