Canonical Allele Identifier: CA397247020
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910916635
gnomAD v3: 17-4631974-G-A
gnomAD v4: 17-4631974-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631974G>A , CM000679.2:g.4631974G>A GRCh38
NC_000017.10:g.4535269G>A , CM000679.1:g.4535269G>A GRCh37
NC_000017.9:g.4482018G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1724C>T MANE Select ENSP00000293761.3:p.Thr575Ile
ENST00000570836.6:c.1724C>T ENSP00000458832.1:p.Thr575Ile
ENST00000293761.7:c.1724C>T ENSP00000293761.3:p.Thr575Ile
ENST00000570836.5:c.1724C>T ENSP00000458832.1:p.Thr575Ile
ENST00000574640.1:c.1607C>T ENSP00000460483.1:p.Thr536Ile
NM_001140.3:c.1724C>T NP_001131.3:p.Thr575Ile
NM_001140.4:c.1724C>T NP_001131.3:p.Thr575Ile
NM_001140.5:c.1724C>T MANE Select NP_001131.3:p.Thr575Ile