Canonical Allele Identifier: CA697253467

Gene: ALOX5AP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30740543T>A , CM000675.2:g.30740543T>A	GRCh38
NC_000013.10:g.31314680T>A , CM000675.1:g.31314680T>A	GRCh37
NC_000013.9:g.30212680T>A	NCBI36
NG_011963.2:g.32066T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.71-3517T>A MANE Select	ENSP00000369858.3:n.71-3517T>A
ENST00000380490.4:c.71-3517T>A	ENSP00000369858.3:n.71-3517T>A
ENST00000617770.4:c.242-3517T>A	ENSP00000479870.1:n.242-3517T>A
NM_001204406.1:c.242-3517T>A	NP_001191335.1:n.242-3517T>A
NM_001629.3:c.71-3517T>A	NP_001620.2:n.71-3517T>A
XM_011535024.1:c.71-3517T>A	XP_011533326.1:n.71-3517T>A
NM_001204406.2:c.242-3517T>A	NP_001191335.1:n.242-3517T>A
NM_001629.4:c.71-3517T>A MANE Select	NP_001620.2:n.71-3517T>A