Canonical Allele Identifier: CA2635535041
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631542-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631542A>C , CM000679.2:g.4631542A>C GRCh38
NC_000017.10:g.4534837A>C , CM000679.1:g.4534837A>C GRCh37
NC_000017.9:g.4481586A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*58T>G MANE Select ENSP00000293761.3:n.*58T>G
ENST00000570836.6:c.*58T>G ENSP00000458832.1:n.*58T>G
ENST00000293761.7:c.*58T>G ENSP00000293761.3:n.*58T>G
ENST00000570836.5:c.*58T>G ENSP00000458832.1:n.*58T>G
ENST00000574640.1:c.*58T>G ENSP00000460483.1:n.*58T>G
NM_001140.3:c.*58T>G NP_001131.3:n.*58T>G
NM_001140.4:c.*58T>G NP_001131.3:n.*58T>G
NM_001140.5:c.*58T>G MANE Select NP_001131.3:n.*58T>G