Canonical Allele Identifier: CA397246882
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535234A>T (hg19) chr17:g.4631939A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631939A>T , CM000679.2:g.4631939A>T GRCh38
NC_000017.10:g.4535234A>T , CM000679.1:g.4535234A>T GRCh37
NC_000017.9:g.4481983A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1759T>A MANE Select ENSP00000293761.3:p.Ser587Thr
ENST00000570836.6:c.1759T>A ENSP00000458832.1:p.Ser587Thr
ENST00000293761.7:c.1759T>A ENSP00000293761.3:p.Ser587Thr
ENST00000570836.5:c.1759T>A ENSP00000458832.1:p.Ser587Thr
ENST00000574640.1:c.1642T>A ENSP00000460483.1:p.Ser548Thr
NM_001140.3:c.1759T>A NP_001131.3:p.Ser587Thr
NM_001140.4:c.1759T>A NP_001131.3:p.Ser587Thr
NM_001140.5:c.1759T>A MANE Select NP_001131.3:p.Ser587Thr
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