Canonical Allele Identifier: CA2808287448
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631505A>C , CM000679.2:g.4631505A>C GRCh38
NC_000017.10:g.4534800A>C , CM000679.1:g.4534800A>C GRCh37
NC_000017.9:g.4481549A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*95T>G MANE Select ENSP00000293761.3:n.*95T>G
ENST00000570836.6:c.*95T>G ENSP00000458832.1:n.*95T>G
ENST00000293761.7:c.*95T>G ENSP00000293761.3:n.*95T>G
ENST00000570836.5:c.*95T>G ENSP00000458832.1:n.*95T>G
ENST00000574640.1:c.*95T>G ENSP00000460483.1:n.*95T>G
NM_001140.3:c.*95T>G NP_001131.3:n.*95T>G
NM_001140.4:c.*95T>G NP_001131.3:n.*95T>G
NM_001140.5:c.*95T>G MANE Select NP_001131.3:n.*95T>G