Canonical Allele Identifier: CA2244455787

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631999T= , CM000679.2:g.4631999T=	GRCh38
NC_000017.10:g.4535294T= , CM000679.1:g.4535294T=	GRCh37
NC_000017.9:g.4482043T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1699A= MANE Select	ENSP00000293761.3:p.Thr567=
ENST00000570836.6:c.1699A=	ENSP00000458832.1:p.Thr567=
ENST00000293761.7:c.1699A=	ENSP00000293761.3:p.Thr567=
ENST00000570836.5:c.1699A=	ENSP00000458832.1:p.Thr567=
ENST00000574640.1:c.1582A=	ENSP00000460483.1:p.Thr528=
NM_001140.3:c.1699A=	NP_001131.3:p.Thr567=
NM_001140.4:c.1699A=	NP_001131.3:p.Thr567=
NM_001140.5:c.1699A= MANE Select	NP_001131.3:p.Thr567=