Canonical Allele Identifier: CA497668215
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4632000-T-G
MyVariant Identifiers: chr17:g.4535295T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4632000T>G , CM000679.2:g.4632000T>G GRCh38
NC_000017.10:g.4535295T>G , CM000679.1:g.4535295T>G GRCh37
NC_000017.9:g.4482044T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1698A>C MANE Select ENSP00000293761.3:p.Pro566=
ENST00000570836.6:c.1698A>C ENSP00000458832.1:p.Pro566=
ENST00000293761.7:c.1698A>C ENSP00000293761.3:p.Pro566=
ENST00000570836.5:c.1698A>C ENSP00000458832.1:p.Pro566=
ENST00000574640.1:c.1581A>C ENSP00000460483.1:p.Pro527=
NM_001140.3:c.1698A>C NP_001131.3:p.Pro566=
NM_001140.4:c.1698A>C NP_001131.3:p.Pro566=
NM_001140.5:c.1698A>C MANE Select NP_001131.3:p.Pro566=
Search 100 bp 5'
Search 100 bp 3'