Canonical Allele Identifier: CA980964878
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910898482
gnomAD v3: 17-4631610-A-ACACTGTTTTCCACCACGCTG
gnomAD v4: 17-4631610-A-ACACTGTTTTCCACCACGCTG
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631611_4631630dup , CM000679.2:g.4631611_4631630dup GRCh38
NC_000017.10:g.4534906_4534925dup , CM000679.1:g.4534906_4534925dup GRCh37
NC_000017.9:g.4481655_4481674dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1959_1978dup MANE Select ENSP00000293761.3:p.Val660AlafsTer28
ENST00000570836.6:c.1959_1978dup ENSP00000458832.1:p.Val660AlafsTer28
ENST00000293761.7:c.1959_1978dup ENSP00000293761.3:p.Val660AlafsTer28
ENST00000570836.5:c.1959_1978dup ENSP00000458832.1:p.Val660AlafsTer28
ENST00000574640.1:c.1842_1861dup ENSP00000460483.1:p.Val621AlafsTer28
NM_001140.3:c.1959_1978dup NP_001131.3:p.Val660AlafsTer28
NM_001140.4:c.1959_1978dup NP_001131.3:p.Val660AlafsTer28
NM_001140.5:c.1959_1978dup MANE Select NP_001131.3:p.Val660AlafsTer28
Search 100 bp 5'
Search 100 bp 3'