Canonical Allele Identifier: CA624854367

Gene: ALOX15

Linked Data

• dbSNP Id: rs1334112696
• gnomAD v2: 17-4534884-G-A
• gnomAD v3: 17-4631589-G-A
• gnomAD v4: 17-4631589-G-A
• MyVariant Identifiers: chr17:g.4534884G>A (hg19) ; chr17:g.4631589G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631589G>A , CM000679.2:g.4631589G>A	GRCh38
NC_000017.10:g.4534884G>A , CM000679.1:g.4534884G>A	GRCh37
NC_000017.9:g.4481633G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*11C>T MANE Select	ENSP00000293761.3:n.*11C>T
ENST00000570836.6:c.*11C>T	ENSP00000458832.1:n.*11C>T
ENST00000293761.7:c.*11C>T	ENSP00000293761.3:n.*11C>T
ENST00000570836.5:c.*11C>T	ENSP00000458832.1:n.*11C>T
ENST00000574640.1:c.*11C>T	ENSP00000460483.1:n.*11C>T
NM_001140.3:c.*11C>T	NP_001131.3:n.*11C>T
NM_001140.4:c.*11C>T	NP_001131.3:n.*11C>T
NM_001140.5:c.*11C>T MANE Select	NP_001131.3:n.*11C>T