Canonical Allele Identifier: CA2082041565

Gene: ALOX5AP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30738637_30738638delinsTG , CM000675.2:g.30738637_30738638delinsTG	GRCh38
NC_000013.10:g.31312774_31312775delinsTG , CM000675.1:g.31312774_31312775delinsTG	GRCh37
NC_000013.9:g.30210774_30210775delinsTG	NCBI36
NG_011963.2:g.30160_30161delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.70+2962_70+2963delinsTG MANE Select	ENSP00000369858.3:n.70+2962_70+2963delinsTG
ENST00000380490.4:c.70+2962_70+2963delinsTG	ENSP00000369858.3:n.70+2962_70+2963delinsTG
ENST00000617770.4:c.241+2962_241+2963delinsTG	ENSP00000479870.1:n.241+2962_241+2963delinsTG
NM_001204406.1:c.241+2962_241+2963delinsTG	NP_001191335.1:n.241+2962_241+2963delinsTG
NM_001629.3:c.70+2962_70+2963delinsTG	NP_001620.2:n.70+2962_70+2963delinsTG
XM_011535024.1:c.70+2962_70+2963delinsTG	XP_011533326.1:n.70+2962_70+2963delinsTG
NM_001204406.2:c.241+2962_241+2963delinsTG	NP_001191335.1:n.241+2962_241+2963delinsTG
NM_001629.4:c.70+2962_70+2963delinsTG MANE Select	NP_001620.2:n.70+2962_70+2963delinsTG