Canonical Allele Identifier: CA397247133

Gene: ALOX15

Linked Data

• gnomAD v4: 17-4631998-G-T
• MyVariant Identifiers: chr17:g.4535293G>T (hg19) ; chr17:g.4631998G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631998G>T , CM000679.2:g.4631998G>T	GRCh38
NC_000017.10:g.4535293G>T , CM000679.1:g.4535293G>T	GRCh37
NC_000017.9:g.4482042G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1700C>A MANE Select	ENSP00000293761.3:p.Thr567Asn
ENST00000570836.6:c.1700C>A	ENSP00000458832.1:p.Thr567Asn
ENST00000293761.7:c.1700C>A	ENSP00000293761.3:p.Thr567Asn
ENST00000570836.5:c.1700C>A	ENSP00000458832.1:p.Thr567Asn
ENST00000574640.1:c.1583C>A	ENSP00000460483.1:p.Thr528Asn
NM_001140.3:c.1700C>A	NP_001131.3:p.Thr567Asn
NM_001140.4:c.1700C>A	NP_001131.3:p.Thr567Asn
NM_001140.5:c.1700C>A MANE Select	NP_001131.3:p.Thr567Asn