Canonical Allele Identifier: CA397246189
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1269621174
gnomAD v2: 17-4534939-C-T
gnomAD v4: 17-4631644-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631644C>T , CM000679.2:g.4631644C>T GRCh38
NC_000017.10:g.4534939C>T , CM000679.1:g.4534939C>T GRCh37
NC_000017.9:g.4481688C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1945G>A MANE Select ENSP00000293761.3:p.Glu649Lys
ENST00000570836.6:c.1945G>A ENSP00000458832.1:p.Glu649Lys
ENST00000293761.7:c.1945G>A ENSP00000293761.3:p.Glu649Lys
ENST00000570836.5:c.1945G>A ENSP00000458832.1:p.Glu649Lys
ENST00000574640.1:c.1828G>A ENSP00000460483.1:p.Glu610Lys
NM_001140.3:c.1945G>A NP_001131.3:p.Glu649Lys
NM_001140.4:c.1945G>A NP_001131.3:p.Glu649Lys
NM_001140.5:c.1945G>A MANE Select NP_001131.3:p.Glu649Lys