Canonical Allele Identifier: CA2635534747
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs2150534132

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631192_4631193insG , CM000679.2:g.4631192_4631193insG GRCh38
NC_000017.10:g.4534487_4534488insG , CM000679.1:g.4534487_4534488insG GRCh37
NC_000017.9:g.4481236_4481237insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*407_*408insC MANE Select ENSP00000293761.3:n.*407_*408insC
ENST00000293761.7:c.*407_*408insC ENSP00000293761.3:n.*407_*408insC
ENST00000570836.5:c.*407_*408insC ENSP00000458832.1:n.*407_*408insC
NM_001140.3:c.*407_*408insC NP_001131.3:n.*407_*408insC
NM_001140.4:c.*407_*408insC NP_001131.3:n.*407_*408insC
NM_001140.5:c.*407_*408insC MANE Select NP_001131.3:n.*407_*408insC