Canonical Allele Identifier: CA497668067

Gene: ALOX15

Linked Data

• MyVariant Identifiers: chr17:g.4535229G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631934G>C , CM000679.2:g.4631934G>C	GRCh38
NC_000017.10:g.4535229G>C , CM000679.1:g.4535229G>C	GRCh37
NC_000017.9:g.4481978G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1764C>G MANE Select	ENSP00000293761.3:p.Leu588=
ENST00000570836.6:c.1764C>G	ENSP00000458832.1:p.Leu588=
ENST00000293761.7:c.1764C>G	ENSP00000293761.3:p.Leu588=
ENST00000570836.5:c.1764C>G	ENSP00000458832.1:p.Leu588=
ENST00000574640.1:c.1647C>G	ENSP00000460483.1:p.Leu549=
NM_001140.3:c.1764C>G	NP_001131.3:p.Leu588=
NM_001140.4:c.1764C>G	NP_001131.3:p.Leu588=
NM_001140.5:c.1764C>G MANE Select	NP_001131.3:p.Leu588=