Canonical Allele Identifier: CA397246830
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535221G>T (hg19) chr17:g.4631926G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631926G>T , CM000679.2:g.4631926G>T GRCh38
NC_000017.10:g.4535221G>T , CM000679.1:g.4535221G>T GRCh37
NC_000017.9:g.4481970G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1772C>A MANE Select ENSP00000293761.3:p.Ser591Tyr
ENST00000570836.6:c.1772C>A ENSP00000458832.1:p.Ser591Tyr
ENST00000293761.7:c.1772C>A ENSP00000293761.3:p.Ser591Tyr
ENST00000570836.5:c.1772C>A ENSP00000458832.1:p.Ser591Tyr
ENST00000574640.1:c.1655C>A ENSP00000460483.1:p.Ser552Tyr
NM_001140.3:c.1772C>A NP_001131.3:p.Ser591Tyr
NM_001140.4:c.1772C>A NP_001131.3:p.Ser591Tyr
NM_001140.5:c.1772C>A MANE Select NP_001131.3:p.Ser591Tyr
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