Canonical Allele Identifier: CA397246871
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535231G>C (hg19) chr17:g.4631936G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631936G>C , CM000679.2:g.4631936G>C GRCh38
NC_000017.10:g.4535231G>C , CM000679.1:g.4535231G>C GRCh37
NC_000017.9:g.4481980G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1762C>G MANE Select ENSP00000293761.3:p.Leu588Val
ENST00000570836.6:c.1762C>G ENSP00000458832.1:p.Leu588Val
ENST00000293761.7:c.1762C>G ENSP00000293761.3:p.Leu588Val
ENST00000570836.5:c.1762C>G ENSP00000458832.1:p.Leu588Val
ENST00000574640.1:c.1645C>G ENSP00000460483.1:p.Leu549Val
NM_001140.3:c.1762C>G NP_001131.3:p.Leu588Val
NM_001140.4:c.1762C>G NP_001131.3:p.Leu588Val
NM_001140.5:c.1762C>G MANE Select NP_001131.3:p.Leu588Val
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