Canonical Allele Identifier: CA2635535046
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631549-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631549C>A , CM000679.2:g.4631549C>A GRCh38
NC_000017.10:g.4534844C>A , CM000679.1:g.4534844C>A GRCh37
NC_000017.9:g.4481593C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*51G>T MANE Select ENSP00000293761.3:n.*51G>T
ENST00000570836.6:c.*51G>T ENSP00000458832.1:n.*51G>T
ENST00000293761.7:c.*51G>T ENSP00000293761.3:n.*51G>T
ENST00000570836.5:c.*51G>T ENSP00000458832.1:n.*51G>T
ENST00000574640.1:c.*51G>T ENSP00000460483.1:n.*51G>T
NM_001140.3:c.*51G>T NP_001131.3:n.*51G>T
NM_001140.4:c.*51G>T NP_001131.3:n.*51G>T
NM_001140.5:c.*51G>T MANE Select NP_001131.3:n.*51G>T