Canonical Allele Identifier: CA497517349

Gene: ALOX15

Linked Data

• dbSNP Id: rs776815094
• gnomAD v4: 17-4631615-G-A
• MyVariant Identifiers: chr17:g.4534910G>A (hg19) ; chr17:g.4631615G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631615G>A , CM000679.2:g.4631615G>A	GRCh38
NC_000017.10:g.4534910G>A , CM000679.1:g.4534910G>A	GRCh37
NC_000017.9:g.4481659G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1974C>T MANE Select	ENSP00000293761.3:p.Asn658=
ENST00000570836.6:c.1974C>T	ENSP00000458832.1:p.Asn658=
ENST00000293761.7:c.1974C>T	ENSP00000293761.3:p.Asn658=
ENST00000570836.5:c.1974C>T	ENSP00000458832.1:p.Asn658=
ENST00000574640.1:c.1857C>T	ENSP00000460483.1:p.Asn619=
NM_001140.3:c.1974C>T	NP_001131.3:p.Asn658=
NM_001140.4:c.1974C>T	NP_001131.3:p.Asn658=
NM_001140.5:c.1974C>T MANE Select	NP_001131.3:p.Asn658=