Canonical Allele Identifier: CA2635534954
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631445-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631445G>T , CM000679.2:g.4631445G>T GRCh38
NC_000017.10:g.4534740G>T , CM000679.1:g.4534740G>T GRCh37
NC_000017.9:g.4481489G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*155C>A MANE Select ENSP00000293761.3:n.*155C>A
ENST00000293761.7:c.*155C>A ENSP00000293761.3:n.*155C>A
ENST00000570836.5:c.*155C>A ENSP00000458832.1:n.*155C>A
ENST00000574640.1:c.*155C>A ENSP00000460483.1:n.*155C>A
NM_001140.3:c.*155C>A NP_001131.3:n.*155C>A
NM_001140.4:c.*155C>A NP_001131.3:n.*155C>A
NM_001140.5:c.*155C>A MANE Select NP_001131.3:n.*155C>A