Canonical Allele Identifier: CA2244455422
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910884354

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631251dup , CM000679.2:g.4631251dup GRCh38
NC_000017.10:g.4534546dup , CM000679.1:g.4534546dup GRCh37
NC_000017.9:g.4481295dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*349dup MANE Select ENSP00000293761.3:n.*349dup
ENST00000293761.7:c.*349dup ENSP00000293761.3:n.*349dup
ENST00000570836.5:c.*349dup ENSP00000458832.1:n.*349dup
NM_001140.3:c.*349dup NP_001131.3:n.*349dup
NM_001140.4:c.*349dup NP_001131.3:n.*349dup
NM_001140.5:c.*349dup MANE Select NP_001131.3:n.*349dup