Canonical Allele Identifier: CA2244455543
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631489_4631490delinsAG , CM000679.2:g.4631489_4631490delinsAG GRCh38
NC_000017.10:g.4534784_4534785delinsAG , CM000679.1:g.4534784_4534785delinsAG GRCh37
NC_000017.9:g.4481533_4481534delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*110_*111delinsCT MANE Select ENSP00000293761.3:n.*110_*111delinsCT
ENST00000570836.6:c.*110_*111delinsCT ENSP00000458832.1:n.*110_*111delinsCT
ENST00000293761.7:c.*110_*111delinsCT ENSP00000293761.3:n.*110_*111delinsCT
ENST00000570836.5:c.*110_*111delinsCT ENSP00000458832.1:n.*110_*111delinsCT
ENST00000574640.1:c.*110_*111delinsCT ENSP00000460483.1:n.*110_*111delinsCT
NM_001140.3:c.*110_*111delinsCT NP_001131.3:n.*110_*111delinsCT
NM_001140.4:c.*110_*111delinsCT NP_001131.3:n.*110_*111delinsCT
NM_001140.5:c.*110_*111delinsCT MANE Select NP_001131.3:n.*110_*111delinsCT