Canonical Allele Identifier: CA397247109
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631993T>G , CM000679.2:g.4631993T>G GRCh38
NC_000017.10:g.4535288T>G , CM000679.1:g.4535288T>G GRCh37
NC_000017.9:g.4482037T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1705A>C MANE Select ENSP00000293761.3:p.Lys569Gln
ENST00000570836.6:c.1705A>C ENSP00000458832.1:p.Lys569Gln
ENST00000293761.7:c.1705A>C ENSP00000293761.3:p.Lys569Gln
ENST00000570836.5:c.1705A>C ENSP00000458832.1:p.Lys569Gln
ENST00000574640.1:c.1588A>C ENSP00000460483.1:p.Lys530Gln
NM_001140.3:c.1705A>C NP_001131.3:p.Lys569Gln
NM_001140.4:c.1705A>C NP_001131.3:p.Lys569Gln
NM_001140.5:c.1705A>C MANE Select NP_001131.3:p.Lys569Gln