Canonical Allele Identifier: CA497668013

Gene: ALOX15

Linked Data

• MyVariant Identifiers: chr17:g.4535214A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631919A>C , CM000679.2:g.4631919A>C	GRCh38
NC_000017.10:g.4535214A>C , CM000679.1:g.4535214A>C	GRCh37
NC_000017.9:g.4481963A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1779T>G MANE Select	ENSP00000293761.3:p.Thr593=
ENST00000570836.6:c.1779T>G	ENSP00000458832.1:p.Thr593=
ENST00000293761.7:c.1779T>G	ENSP00000293761.3:p.Thr593=
ENST00000570836.5:c.1779T>G	ENSP00000458832.1:p.Thr593=
ENST00000574640.1:c.1662T>G	ENSP00000460483.1:p.Thr554=
NM_001140.3:c.1779T>G	NP_001131.3:p.Thr593=
NM_001140.4:c.1779T>G	NP_001131.3:p.Thr593=
NM_001140.5:c.1779T>G MANE Select	NP_001131.3:p.Thr593=