Canonical Allele Identifier: CA772438118

Gene: ALOX15

Linked Data

• dbSNP Id: rs1249146126
• MyVariant Identifiers: chr17:g.4535298_4535299insG (hg19) ; chr17:g.4632003_4632004insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4632008dup , CM000679.2:g.4632008dup	GRCh38
NC_000017.10:g.4535303dup , CM000679.1:g.4535303dup	GRCh37
NC_000017.9:g.4482052dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1694dup MANE Select	ENSP00000293761.3:p.Pro566AlafsTer?
ENST00000570836.6:c.1694dup	ENSP00000458832.1:p.Pro566AlafsTer?
ENST00000293761.7:c.1694dup	ENSP00000293761.3:p.Pro566AlafsTer?
ENST00000570836.5:c.1694dup	ENSP00000458832.1:p.Pro566AlafsTer?
ENST00000574640.1:c.1577dup	ENSP00000460483.1:p.Pro527AlafsTer?
NM_001140.3:c.1694dup	NP_001131.3:p.Pro566AlafsTer?
NM_001140.4:c.1694dup	NP_001131.3:p.Pro566AlafsTer?
NM_001140.5:c.1694dup MANE Select	NP_001131.3:p.Pro566AlafsTer?