Canonical Allele Identifier: CA2244455629

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631647A= , CM000679.2:g.4631647A=	GRCh38
NC_000017.10:g.4534942A= , CM000679.1:g.4534942A=	GRCh37
NC_000017.9:g.4481691A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1942T= MANE Select	ENSP00000293761.3:p.Tyr648=
ENST00000570836.6:c.1942T=	ENSP00000458832.1:p.Tyr648=
ENST00000293761.7:c.1942T=	ENSP00000293761.3:p.Tyr648=
ENST00000570836.5:c.1942T=	ENSP00000458832.1:p.Tyr648=
ENST00000574640.1:c.1825T=	ENSP00000460483.1:p.Tyr609=
NM_001140.3:c.1942T=	NP_001131.3:p.Tyr648=
NM_001140.4:c.1942T=	NP_001131.3:p.Tyr648=
NM_001140.5:c.1942T= MANE Select	NP_001131.3:p.Tyr648=