Canonical Allele Identifier: CA2244455725

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631864_4631867delinsAGGG , CM000679.2:g.4631864_4631867delinsAGGG	GRCh38
NC_000017.10:g.4535159_4535162delinsAGGG , CM000679.1:g.4535159_4535162delinsAGGG	GRCh37
NC_000017.9:g.4481908_4481911delinsAGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1809+22_1809+25delinsCCCT MANE Select	ENSP00000293761.3:n.1809+22_1809+25delinsCCCT
ENST00000570836.6:c.1809+22_1809+25delinsCCCT	ENSP00000458832.1:n.1809+22_1809+25delinsCCCT
ENST00000293761.7:c.1809+22_1809+25delinsCCCT	ENSP00000293761.3:n.1809+22_1809+25delinsCCCT
ENST00000570836.5:c.1809+22_1809+25delinsCCCT	ENSP00000458832.1:n.1809+22_1809+25delinsCCCT
ENST00000574640.1:c.1692+22_1692+25delinsCCCT	ENSP00000460483.1:n.1692+22_1692+25delinsCCCT
NM_001140.3:c.1809+22_1809+25delinsCCCT	NP_001131.3:n.1809+22_1809+25delinsCCCT
NM_001140.4:c.1809+22_1809+25delinsCCCT	NP_001131.3:n.1809+22_1809+25delinsCCCT
NM_001140.5:c.1809+22_1809+25delinsCCCT MANE Select	NP_001131.3:n.1809+22_1809+25delinsCCCT