Canonical Allele Identifier: CA8306688
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs772605354
gnomAD v2: 17-4535240-G-C
gnomAD v4: 17-4631945-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631945G>C , CM000679.2:g.4631945G>C GRCh38
NC_000017.10:g.4535240G>C , CM000679.1:g.4535240G>C GRCh37
NC_000017.9:g.4481989G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1753C>G MANE Select ENSP00000293761.3:p.Gln585Glu
ENST00000570836.6:c.1753C>G ENSP00000458832.1:p.Gln585Glu
ENST00000293761.7:c.1753C>G ENSP00000293761.3:p.Gln585Glu
ENST00000570836.5:c.1753C>G ENSP00000458832.1:p.Gln585Glu
ENST00000574640.1:c.1636C>G ENSP00000460483.1:p.Gln546Glu
NM_001140.3:c.1753C>G NP_001131.3:p.Gln585Glu
NM_001140.4:c.1753C>G NP_001131.3:p.Gln585Glu
NM_001140.5:c.1753C>G MANE Select NP_001131.3:p.Gln585Glu