Canonical Allele Identifier: CA8306698
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs770801037

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631999_4632005del , CM000679.2:g.4631999_4632005del GRCh38
NC_000017.10:g.4535294_4535300del , CM000679.1:g.4535294_4535300del GRCh37
NC_000017.9:g.4482043_4482049del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1695_1701del MANE Select ENSP00000293761.3:p.Thr567ArgfsTer8
ENST00000570836.6:c.1695_1701del ENSP00000458832.1:p.Thr567ArgfsTer8
ENST00000293761.7:c.1695_1701del ENSP00000293761.3:p.Thr567ArgfsTer8
ENST00000570836.5:c.1695_1701del ENSP00000458832.1:p.Thr567ArgfsTer8
ENST00000574640.1:c.1578_1584del ENSP00000460483.1:p.Thr528ArgfsTer8
NM_001140.3:c.1695_1701del NP_001131.3:p.Thr567ArgfsTer8
NM_001140.4:c.1695_1701del NP_001131.3:p.Thr567ArgfsTer8
NM_001140.5:c.1695_1701del MANE Select NP_001131.3:p.Thr567ArgfsTer8