Canonical Allele Identifier: CA287133166
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs909215074
MyVariant Identifiers: chr17:g.4535258T>G (hg19) chr17:g.4631963T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631963T>G , CM000679.2:g.4631963T>G GRCh38
NC_000017.10:g.4535258T>G , CM000679.1:g.4535258T>G GRCh37
NC_000017.9:g.4482007T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1735A>C MANE Select ENSP00000293761.3:p.Thr579Pro
ENST00000570836.6:c.1735A>C ENSP00000458832.1:p.Thr579Pro
ENST00000293761.7:c.1735A>C ENSP00000293761.3:p.Thr579Pro
ENST00000570836.5:c.1735A>C ENSP00000458832.1:p.Thr579Pro
ENST00000574640.1:c.1618A>C ENSP00000460483.1:p.Thr540Pro
NM_001140.3:c.1735A>C NP_001131.3:p.Thr579Pro
NM_001140.4:c.1735A>C NP_001131.3:p.Thr579Pro
NM_001140.5:c.1735A>C MANE Select NP_001131.3:p.Thr579Pro
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