Canonical Allele Identifier: CA287132926

Gene: ALOX15

Linked Data

• dbSNP Id: rs1013958289
• gnomAD v3: 17-4631531-C-T
• gnomAD v4: 17-4631531-C-T
• MyVariant Identifiers: chr17:g.4534826C>T (hg19) ; chr17:g.4631531C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631531C>T , CM000679.2:g.4631531C>T	GRCh38
NC_000017.10:g.4534826C>T , CM000679.1:g.4534826C>T	GRCh37
NC_000017.9:g.4481575C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*69G>A MANE Select	ENSP00000293761.3:n.*69G>A
ENST00000570836.6:c.*69G>A	ENSP00000458832.1:n.*69G>A
ENST00000293761.7:c.*69G>A	ENSP00000293761.3:n.*69G>A
ENST00000570836.5:c.*69G>A	ENSP00000458832.1:n.*69G>A
ENST00000574640.1:c.*69G>A	ENSP00000460483.1:n.*69G>A
NM_001140.3:c.*69G>A	NP_001131.3:n.*69G>A
NM_001140.4:c.*69G>A	NP_001131.3:n.*69G>A
NM_001140.5:c.*69G>A MANE Select	NP_001131.3:n.*69G>A