Canonical Allele Identifier: CA2635535019
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631519-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631519G>T , CM000679.2:g.4631519G>T GRCh38
NC_000017.10:g.4534814G>T , CM000679.1:g.4534814G>T GRCh37
NC_000017.9:g.4481563G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*81C>A MANE Select ENSP00000293761.3:n.*81C>A
ENST00000570836.6:c.*81C>A ENSP00000458832.1:n.*81C>A
ENST00000293761.7:c.*81C>A ENSP00000293761.3:n.*81C>A
ENST00000570836.5:c.*81C>A ENSP00000458832.1:n.*81C>A
ENST00000574640.1:c.*81C>A ENSP00000460483.1:n.*81C>A
NM_001140.3:c.*81C>A NP_001131.3:n.*81C>A
NM_001140.4:c.*81C>A NP_001131.3:n.*81C>A
NM_001140.5:c.*81C>A MANE Select NP_001131.3:n.*81C>A
Search 100 bp 5'
Search 100 bp 3'