Canonical Allele Identifier: CA2244455609
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631610A= , CM000679.2:g.4631610A= GRCh38
NC_000017.10:g.4534905A= , CM000679.1:g.4534905A= GRCh37
NC_000017.9:g.4481654A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1979T= MANE Select ENSP00000293761.3:p.Val660=
ENST00000570836.6:c.1979T= ENSP00000458832.1:p.Val660=
ENST00000293761.7:c.1979T= ENSP00000293761.3:p.Val660=
ENST00000570836.5:c.1979T= ENSP00000458832.1:p.Val660=
ENST00000574640.1:c.1862T= ENSP00000460483.1:p.Val621=
NM_001140.3:c.1979T= NP_001131.3:p.Val660=
NM_001140.4:c.1979T= NP_001131.3:p.Val660=
NM_001140.5:c.1979T= MANE Select NP_001131.3:p.Val660=