Canonical Allele Identifier: CA397246569
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631751T>A , CM000679.2:g.4631751T>A GRCh38
NC_000017.10:g.4535046T>A , CM000679.1:g.4535046T>A GRCh37
NC_000017.9:g.4481795T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1838A>T MANE Select ENSP00000293761.3:p.Tyr613Phe
ENST00000570836.6:c.1838A>T ENSP00000458832.1:p.Tyr613Phe
ENST00000293761.7:c.1838A>T ENSP00000293761.3:p.Tyr613Phe
ENST00000570836.5:c.1838A>T ENSP00000458832.1:p.Tyr613Phe
ENST00000574640.1:c.1721A>T ENSP00000460483.1:p.Tyr574Phe
NM_001140.3:c.1838A>T NP_001131.3:p.Tyr613Phe
NM_001140.4:c.1838A>T NP_001131.3:p.Tyr613Phe
NM_001140.5:c.1838A>T MANE Select NP_001131.3:p.Tyr613Phe