Canonical Allele Identifier: CA287132830

Gene: ALOX15

Linked Data

• dbSNP Id: rs539035649
• gnomAD v2: 17-4534532-C-A
• gnomAD v3: 17-4631237-C-A
• gnomAD v4: 17-4631237-C-A
• MyVariant Identifiers: chr17:g.4534532C>A (hg19) ; chr17:g.4631237C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631237C>A , CM000679.2:g.4631237C>A	GRCh38
NC_000017.10:g.4534532C>A , CM000679.1:g.4534532C>A	GRCh37
NC_000017.9:g.4481281C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*363G>T MANE Select	ENSP00000293761.3:n.*363G>T
ENST00000293761.7:c.*363G>T	ENSP00000293761.3:n.*363G>T
ENST00000570836.5:c.*363G>T	ENSP00000458832.1:n.*363G>T
NM_001140.3:c.*363G>T	NP_001131.3:n.*363G>T
NM_001140.4:c.*363G>T	NP_001131.3:n.*363G>T
NM_001140.5:c.*363G>T MANE Select	NP_001131.3:n.*363G>T