Canonical Allele Identifier: CA2244455778
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631984_4631988delinsTTGCA , CM000679.2:g.4631984_4631988delinsTTGCA GRCh38
NC_000017.10:g.4535279_4535283delinsTTGCA , CM000679.1:g.4535279_4535283delinsTTGCA GRCh37
NC_000017.9:g.4482028_4482032delinsTTGCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1710_1714delinsTGCAA MANE Select ENSP00000293761.3:p.Asp570=
ENST00000570836.6:c.1710_1714delinsTGCAA ENSP00000458832.1:p.Asp570=
ENST00000293761.7:c.1710_1714delinsTGCAA ENSP00000293761.3:p.Asp570=
ENST00000570836.5:c.1710_1714delinsTGCAA ENSP00000458832.1:p.Asp570=
ENST00000574640.1:c.1593_1597delinsTGCAA ENSP00000460483.1:p.Asp531=
NM_001140.3:c.1710_1714delinsTGCAA NP_001131.3:p.Asp570=
NM_001140.4:c.1710_1714delinsTGCAA NP_001131.3:p.Asp570=
NM_001140.5:c.1710_1714delinsTGCAA MANE Select NP_001131.3:p.Asp570=