Canonical Allele Identifier: CA2635535091
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631864_4631865dup , CM000679.2:g.4631864_4631865dup GRCh38
NC_000017.10:g.4535159_4535160dup , CM000679.1:g.4535159_4535160dup GRCh37
NC_000017.9:g.4481908_4481909dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1809+24_1809+25dup MANE Select ENSP00000293761.3:n.1809+24_1809+25dup
ENST00000570836.6:c.1809+24_1809+25dup ENSP00000458832.1:n.1809+24_1809+25dup
ENST00000293761.7:c.1809+24_1809+25dup ENSP00000293761.3:n.1809+24_1809+25dup
ENST00000570836.5:c.1809+24_1809+25dup ENSP00000458832.1:n.1809+24_1809+25dup
ENST00000574640.1:c.1692+24_1692+25dup ENSP00000460483.1:n.1692+24_1692+25dup
NM_001140.3:c.1809+24_1809+25dup NP_001131.3:n.1809+24_1809+25dup
NM_001140.4:c.1809+24_1809+25dup NP_001131.3:n.1809+24_1809+25dup
NM_001140.5:c.1809+24_1809+25dup MANE Select NP_001131.3:n.1809+24_1809+25dup