Canonical Allele Identifier: CA8306621
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs770087312
ExAC: 17:4534921 C / T
gnomAD v2: 17-4534921-C-T
gnomAD v3: 17-4631626-C-T
gnomAD v4: 17-4631626-C-T
MyVariant Identifiers: chr17:g.4534921C>T (hg19) chr17:g.4631626C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631626C>T , CM000679.2:g.4631626C>T GRCh38
NC_000017.10:g.4534921C>T , CM000679.1:g.4534921C>T GRCh37
NC_000017.9:g.4481670C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1963G>A MANE Select ENSP00000293761.3:p.Val655Met
ENST00000570836.6:c.1963G>A ENSP00000458832.1:p.Val655Met
ENST00000293761.7:c.1963G>A ENSP00000293761.3:p.Val655Met
ENST00000570836.5:c.1963G>A ENSP00000458832.1:p.Val655Met
ENST00000574640.1:c.1846G>A ENSP00000460483.1:p.Val616Met
NM_001140.3:c.1963G>A NP_001131.3:p.Val655Met
NM_001140.4:c.1963G>A NP_001131.3:p.Val655Met
NM_001140.5:c.1963G>A MANE Select NP_001131.3:p.Val655Met
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