Canonical Allele Identifier: CA2635534748

Gene: ALOX15

Linked Data

• dbSNP Id: rs2150534134
• gnomAD v4: 17-4631193-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631193_4631194insCG , CM000679.2:g.4631193_4631194insCG	GRCh38
NC_000017.10:g.4534488_4534489insCG , CM000679.1:g.4534488_4534489insCG	GRCh37
NC_000017.9:g.4481237_4481238insCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*406_*407insCG MANE Select	ENSP00000293761.3:n.*406_*407insCG
ENST00000293761.7:c.*406_*407insCG	ENSP00000293761.3:n.*406_*407insCG
ENST00000570836.5:c.*406_*407insCG	ENSP00000458832.1:n.*406_*407insCG
NM_001140.3:c.*406_*407insCG	NP_001131.3:n.*406_*407insCG
NM_001140.4:c.*406_*407insCG	NP_001131.3:n.*406_*407insCG
NM_001140.5:c.*406_*407insCG MANE Select	NP_001131.3:n.*406_*407insCG