Canonical Allele Identifier: CA8306692
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs149366613
ExAC: 17:4535260 G / A
gnomAD v2: 17-4535260-G-A
gnomAD v3: 17-4631965-G-A
gnomAD v4: 17-4631965-G-A
MyVariant Identifiers: chr17:g.4535260G>A (hg19) chr17:g.4631965G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631965G>A , CM000679.2:g.4631965G>A GRCh38
NC_000017.10:g.4535260G>A , CM000679.1:g.4535260G>A GRCh37
NC_000017.9:g.4482009G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1733C>T MANE Select ENSP00000293761.3:p.Ala578Val
ENST00000570836.6:c.1733C>T ENSP00000458832.1:p.Ala578Val
ENST00000293761.7:c.1733C>T ENSP00000293761.3:p.Ala578Val
ENST00000570836.5:c.1733C>T ENSP00000458832.1:p.Ala578Val
ENST00000574640.1:c.1616C>T ENSP00000460483.1:p.Ala539Val
NM_001140.3:c.1733C>T NP_001131.3:p.Ala578Val
NM_001140.4:c.1733C>T NP_001131.3:p.Ala578Val
NM_001140.5:c.1733C>T MANE Select NP_001131.3:p.Ala578Val
Search 100 bp 5'
Search 100 bp 3'