Canonical Allele Identifier: CA497518276

Gene: ALOX15

Linked Data

• MyVariant Identifiers: chr17:g.4535021A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631726A>G , CM000679.2:g.4631726A>G	GRCh38
NC_000017.10:g.4535021A>G , CM000679.1:g.4535021A>G	GRCh37
NC_000017.9:g.4481770A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1863T>C MANE Select	ENSP00000293761.3:p.Ala621=
ENST00000570836.6:c.1863T>C	ENSP00000458832.1:p.Ala621=
ENST00000293761.7:c.1863T>C	ENSP00000293761.3:p.Ala621=
ENST00000570836.5:c.1863T>C	ENSP00000458832.1:p.Ala621=
ENST00000574640.1:c.1746T>C	ENSP00000460483.1:p.Ala582=
NM_001140.3:c.1863T>C	NP_001131.3:p.Ala621=
NM_001140.4:c.1863T>C	NP_001131.3:p.Ala621=
NM_001140.5:c.1863T>C MANE Select	NP_001131.3:p.Ala621=