Canonical Allele Identifier: CA2635534709
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631153-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631153C>T , CM000679.2:g.4631153C>T GRCh38
NC_000017.10:g.4534448C>T , CM000679.1:g.4534448C>T GRCh37
NC_000017.9:g.4481197C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*447G>A MANE Select ENSP00000293761.3:n.*447G>A
ENST00000293761.7:c.*447G>A ENSP00000293761.3:n.*447G>A
ENST00000570836.5:c.*447G>A ENSP00000458832.1:n.*447G>A
NM_001140.3:c.*447G>A NP_001131.3:n.*447G>A
NM_001140.4:c.*447G>A NP_001131.3:n.*447G>A
NM_001140.5:c.*447G>A MANE Select NP_001131.3:n.*447G>A
Search 100 bp 5'
Search 100 bp 3'