Canonical Allele Identifier: CA2635535050
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631556-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631556T>C , CM000679.2:g.4631556T>C GRCh38
NC_000017.10:g.4534851T>C , CM000679.1:g.4534851T>C GRCh37
NC_000017.9:g.4481600T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*44A>G MANE Select ENSP00000293761.3:n.*44A>G
ENST00000570836.6:c.*44A>G ENSP00000458832.1:n.*44A>G
ENST00000293761.7:c.*44A>G ENSP00000293761.3:n.*44A>G
ENST00000570836.5:c.*44A>G ENSP00000458832.1:n.*44A>G
ENST00000574640.1:c.*44A>G ENSP00000460483.1:n.*44A>G
NM_001140.3:c.*44A>G NP_001131.3:n.*44A>G
NM_001140.4:c.*44A>G NP_001131.3:n.*44A>G
NM_001140.5:c.*44A>G MANE Select NP_001131.3:n.*44A>G