Canonical Allele Identifier: CA2082041644

Gene: ALOX5AP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30738709_30738710delinsCT , CM000675.2:g.30738709_30738710delinsCT	GRCh38
NC_000013.10:g.31312846_31312847delinsCT , CM000675.1:g.31312846_31312847delinsCT	GRCh37
NC_000013.9:g.30210846_30210847delinsCT	NCBI36
NG_011963.2:g.30232_30233delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.70+3034_70+3035delinsCT MANE Select	ENSP00000369858.3:n.70+3034_70+3035delinsCT
ENST00000380490.4:c.70+3034_70+3035delinsCT	ENSP00000369858.3:n.70+3034_70+3035delinsCT
ENST00000617770.4:c.241+3034_241+3035delinsCT	ENSP00000479870.1:n.241+3034_241+3035delinsCT
NM_001204406.1:c.241+3034_241+3035delinsCT	NP_001191335.1:n.241+3034_241+3035delinsCT
NM_001629.3:c.70+3034_70+3035delinsCT	NP_001620.2:n.70+3034_70+3035delinsCT
XM_011535024.1:c.70+3034_70+3035delinsCT	XP_011533326.1:n.70+3034_70+3035delinsCT
NM_001204406.2:c.241+3034_241+3035delinsCT	NP_001191335.1:n.241+3034_241+3035delinsCT
NM_001629.4:c.70+3034_70+3035delinsCT MANE Select	NP_001620.2:n.70+3034_70+3035delinsCT