Canonical Allele Identifier: CA397246852
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631931C>A , CM000679.2:g.4631931C>A GRCh38
NC_000017.10:g.4535226C>A , CM000679.1:g.4535226C>A GRCh37
NC_000017.9:g.4481975C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1767G>T MANE Select ENSP00000293761.3:p.Gln589His
ENST00000570836.6:c.1767G>T ENSP00000458832.1:p.Gln589His
ENST00000293761.7:c.1767G>T ENSP00000293761.3:p.Gln589His
ENST00000570836.5:c.1767G>T ENSP00000458832.1:p.Gln589His
ENST00000574640.1:c.1650G>T ENSP00000460483.1:p.Gln550His
NM_001140.3:c.1767G>T NP_001131.3:p.Gln589His
NM_001140.4:c.1767G>T NP_001131.3:p.Gln589His
NM_001140.5:c.1767G>T MANE Select NP_001131.3:p.Gln589His