Canonical Allele Identifier: CA397246140
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631629T>C , CM000679.2:g.4631629T>C GRCh38
NC_000017.10:g.4534924T>C , CM000679.1:g.4534924T>C GRCh37
NC_000017.9:g.4481673T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1960A>G MANE Select ENSP00000293761.3:p.Ser654Gly
ENST00000570836.6:c.1960A>G ENSP00000458832.1:p.Ser654Gly
ENST00000293761.7:c.1960A>G ENSP00000293761.3:p.Ser654Gly
ENST00000570836.5:c.1960A>G ENSP00000458832.1:p.Ser654Gly
ENST00000574640.1:c.1843A>G ENSP00000460483.1:p.Ser615Gly
NM_001140.3:c.1960A>G NP_001131.3:p.Ser654Gly
NM_001140.4:c.1960A>G NP_001131.3:p.Ser654Gly
NM_001140.5:c.1960A>G MANE Select NP_001131.3:p.Ser654Gly