Canonical Allele Identifier: CA2635534752
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs2150534135

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631195_4631196insGATGA , CM000679.2:g.4631195_4631196insGATGA GRCh38
NC_000017.10:g.4534490_4534491insGATGA , CM000679.1:g.4534490_4534491insGATGA GRCh37
NC_000017.9:g.4481239_4481240insGATGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*404_*405insTCATC MANE Select ENSP00000293761.3:n.*404_*405insTCATC
ENST00000293761.7:c.*404_*405insTCATC ENSP00000293761.3:n.*404_*405insTCATC
ENST00000570836.5:c.*404_*405insTCATC ENSP00000458832.1:n.*404_*405insTCATC
NM_001140.3:c.*404_*405insTCATC NP_001131.3:n.*404_*405insTCATC
NM_001140.4:c.*404_*405insTCATC NP_001131.3:n.*404_*405insTCATC
NM_001140.5:c.*404_*405insTCATC MANE Select NP_001131.3:n.*404_*405insTCATC