Canonical Allele Identifier: CA2635534884
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631346-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631346T>G , CM000679.2:g.4631346T>G GRCh38
NC_000017.10:g.4534641T>G , CM000679.1:g.4534641T>G GRCh37
NC_000017.9:g.4481390T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*254A>C MANE Select ENSP00000293761.3:n.*254A>C
ENST00000293761.7:c.*254A>C ENSP00000293761.3:n.*254A>C
ENST00000570836.5:c.*254A>C ENSP00000458832.1:n.*254A>C
ENST00000574640.1:c.*254A>C ENSP00000460483.1:n.*254A>C
NM_001140.3:c.*254A>C NP_001131.3:n.*254A>C
NM_001140.4:c.*254A>C NP_001131.3:n.*254A>C
NM_001140.5:c.*254A>C MANE Select NP_001131.3:n.*254A>C