Canonical Allele Identifier: CA2244455577
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631561_4631567delinsTGGGTGA , CM000679.2:g.4631561_4631567delinsTGGGTGA GRCh38
NC_000017.10:g.4534856_4534862delinsTGGGTGA , CM000679.1:g.4534856_4534862delinsTGGGTGA GRCh37
NC_000017.9:g.4481605_4481611delinsTGGGTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*33_*39delinsTCACCCA MANE Select ENSP00000293761.3:n.*33_*39delinsTCACCCA
ENST00000570836.6:c.*33_*39delinsTCACCCA ENSP00000458832.1:n.*33_*39delinsTCACCCA
ENST00000293761.7:c.*33_*39delinsTCACCCA ENSP00000293761.3:n.*33_*39delinsTCACCCA
ENST00000570836.5:c.*33_*39delinsTCACCCA ENSP00000458832.1:n.*33_*39delinsTCACCCA
ENST00000574640.1:c.*33_*39delinsTCACCCA ENSP00000460483.1:n.*33_*39delinsTCACCCA
NM_001140.3:c.*33_*39delinsTCACCCA NP_001131.3:n.*33_*39delinsTCACCCA
NM_001140.4:c.*33_*39delinsTCACCCA NP_001131.3:n.*33_*39delinsTCACCCA
NM_001140.5:c.*33_*39delinsTCACCCA MANE Select NP_001131.3:n.*33_*39delinsTCACCCA