Canonical Allele Identifier: CA2635534758
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631206-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631206T>G , CM000679.2:g.4631206T>G GRCh38
NC_000017.10:g.4534501T>G , CM000679.1:g.4534501T>G GRCh37
NC_000017.9:g.4481250T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*394A>C MANE Select ENSP00000293761.3:n.*394A>C
ENST00000293761.7:c.*394A>C ENSP00000293761.3:n.*394A>C
ENST00000570836.5:c.*394A>C ENSP00000458832.1:n.*394A>C
NM_001140.3:c.*394A>C NP_001131.3:n.*394A>C
NM_001140.4:c.*394A>C NP_001131.3:n.*394A>C
NM_001140.5:c.*394A>C MANE Select NP_001131.3:n.*394A>C
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