Canonical Allele Identifier: CA2635535042
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631543-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631543A>G , CM000679.2:g.4631543A>G GRCh38
NC_000017.10:g.4534838A>G , CM000679.1:g.4534838A>G GRCh37
NC_000017.9:g.4481587A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*57T>C MANE Select ENSP00000293761.3:n.*57T>C
ENST00000570836.6:c.*57T>C ENSP00000458832.1:n.*57T>C
ENST00000293761.7:c.*57T>C ENSP00000293761.3:n.*57T>C
ENST00000570836.5:c.*57T>C ENSP00000458832.1:n.*57T>C
ENST00000574640.1:c.*57T>C ENSP00000460483.1:n.*57T>C
NM_001140.3:c.*57T>C NP_001131.3:n.*57T>C
NM_001140.4:c.*57T>C NP_001131.3:n.*57T>C
NM_001140.5:c.*57T>C MANE Select NP_001131.3:n.*57T>C