Canonical Allele Identifier: CA2244455391
Gene: ALOX15 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631181G= , CM000679.2:g.4631181G= GRCh38
NC_000017.10:g.4534476G= , CM000679.1:g.4534476G= GRCh37
NC_000017.9:g.4481225G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*419C= MANE Select ENSP00000293761.3:n.*419C=
ENST00000293761.7:c.*419C= ENSP00000293761.3:n.*419C=
ENST00000570836.5:c.*419C= ENSP00000458832.1:n.*419C=
NM_001140.3:c.*419C= NP_001131.3:n.*419C=
NM_001140.4:c.*419C= NP_001131.3:n.*419C=
NM_001140.5:c.*419C= MANE Select NP_001131.3:n.*419C=
Search 100 bp 5'
Search 100 bp 3'