Canonical Allele Identifier: CA2244455462
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631352_4631362delinsTGAAGAAAGAG , CM000679.2:g.4631352_4631362delinsTGAAGAAAGAG GRCh38
NC_000017.10:g.4534647_4534657delinsTGAAGAAAGAG , CM000679.1:g.4534647_4534657delinsTGAAGAAAGAG GRCh37
NC_000017.9:g.4481396_4481406delinsTGAAGAAAGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*238_*248delinsCTCTTTCTTCA MANE Select ENSP00000293761.3:n.*238_*248delinsCTCTTTCTTCA
ENST00000293761.7:c.*238_*248delinsCTCTTTCTTCA ENSP00000293761.3:n.*238_*248delinsCTCTTTCTTCA
ENST00000570836.5:c.*238_*248delinsCTCTTTCTTCA ENSP00000458832.1:n.*238_*248delinsCTCTTTCTTCA
ENST00000574640.1:c.*238_*248delinsCTCTTTCTTCA ENSP00000460483.1:n.*238_*248delinsCTCTTTCTTCA
NM_001140.3:c.*238_*248delinsCTCTTTCTTCA NP_001131.3:n.*238_*248delinsCTCTTTCTTCA
NM_001140.4:c.*238_*248delinsCTCTTTCTTCA NP_001131.3:n.*238_*248delinsCTCTTTCTTCA
NM_001140.5:c.*238_*248delinsCTCTTTCTTCA MANE Select NP_001131.3:n.*238_*248delinsCTCTTTCTTCA