Canonical Allele Identifier: CA397246631

Gene: ALOX15

Linked Data

• MyVariant Identifiers: chr17:g.4535062G>C (hg19) ; chr17:g.4631767G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631767G>C , CM000679.2:g.4631767G>C	GRCh38
NC_000017.10:g.4535062G>C , CM000679.1:g.4535062G>C	GRCh37
NC_000017.9:g.4481811G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1822C>G MANE Select	ENSP00000293761.3:p.Gln608Glu
ENST00000570836.6:c.1822C>G	ENSP00000458832.1:p.Gln608Glu
ENST00000293761.7:c.1822C>G	ENSP00000293761.3:p.Gln608Glu
ENST00000570836.5:c.1822C>G	ENSP00000458832.1:p.Gln608Glu
ENST00000574640.1:c.1705C>G	ENSP00000460483.1:p.Gln569Glu
NM_001140.3:c.1822C>G	NP_001131.3:p.Gln608Glu
NM_001140.4:c.1822C>G	NP_001131.3:p.Gln608Glu
NM_001140.5:c.1822C>G MANE Select	NP_001131.3:p.Gln608Glu