Canonical Allele Identifier: CA8306696
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs764593975
ExAC: 17:4535279 T / G
gnomAD v2: 17-4535279-T-G
gnomAD v4: 17-4631984-T-G
MyVariant Identifiers: chr17:g.4535279T>G (hg19) chr17:g.4631984T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631984T>G , CM000679.2:g.4631984T>G GRCh38
NC_000017.10:g.4535279T>G , CM000679.1:g.4535279T>G GRCh37
NC_000017.9:g.4482028T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1714A>C MANE Select ENSP00000293761.3:p.Thr572Pro
ENST00000570836.6:c.1714A>C ENSP00000458832.1:p.Thr572Pro
ENST00000293761.7:c.1714A>C ENSP00000293761.3:p.Thr572Pro
ENST00000570836.5:c.1714A>C ENSP00000458832.1:p.Thr572Pro
ENST00000574640.1:c.1597A>C ENSP00000460483.1:p.Thr533Pro
NM_001140.3:c.1714A>C NP_001131.3:p.Thr572Pro
NM_001140.4:c.1714A>C NP_001131.3:p.Thr572Pro
NM_001140.5:c.1714A>C MANE Select NP_001131.3:p.Thr572Pro
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