Canonical Allele Identifier: CA2635534972
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631462-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631462A>T , CM000679.2:g.4631462A>T GRCh38
NC_000017.10:g.4534757A>T , CM000679.1:g.4534757A>T GRCh37
NC_000017.9:g.4481506A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*138T>A MANE Select ENSP00000293761.3:n.*138T>A
ENST00000293761.7:c.*138T>A ENSP00000293761.3:n.*138T>A
ENST00000570836.5:c.*138T>A ENSP00000458832.1:n.*138T>A
ENST00000574640.1:c.*138T>A ENSP00000460483.1:n.*138T>A
NM_001140.3:c.*138T>A NP_001131.3:n.*138T>A
NM_001140.4:c.*138T>A NP_001131.3:n.*138T>A
NM_001140.5:c.*138T>A MANE Select NP_001131.3:n.*138T>A