Canonical Allele Identifier: CA1906904501

Gene: ALOX5

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.45396036A>T , CM000672.2:g.45396036A>T	GRCh38
NC_000010.10:g.45891484A>T , CM000672.1:g.45891484A>T	GRCh37
NC_000010.9:g.45211490A>T	NCBI36
NG_011437.1:g.26856A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374391.7:c.431+100A>T MANE Select	ENSP00000363512.2:n.431+100A>T
ENST00000374391.6:c.431+100A>T	ENSP00000363512.2:n.431+100A>T
ENST00000542434.5:c.431+100A>T	ENSP00000437634.1:n.431+100A>T
ENST00000612635.4:c.349+13355A>T	ENSP00000483803.1:n.349+13355A>T
NM_000698.3:c.431+100A>T	NP_000689.1:n.431+100A>T
NM_001256153.1:c.431+100A>T	NP_001243082.1:n.431+100A>T
NM_001256154.1:c.431+100A>T	NP_001243083.1:n.431+100A>T
XM_011539564.1:c.431+100A>T	XP_011537866.1:n.431+100A>T
NM_000698.4:c.431+100A>T	NP_000689.1:n.431+100A>T
NM_001256153.2:c.431+100A>T	NP_001243082.1:n.431+100A>T
NM_001256154.2:c.431+100A>T	NP_001243083.1:n.431+100A>T
NM_001320861.1:c.431+100A>T	NP_001307790.1:n.431+100A>T
NM_001320862.1:c.-5+100A>T	NP_001307791.1:n.-5+100A>T
XM_017016012.1:c.-5+13355A>T	XP_016871501.1:n.-5+13355A>T
XR_001747075.1:n.498+100A>T
NM_000698.5:c.431+100A>T MANE Select	NP_000689.1:n.431+100A>T
NM_001256153.3:c.431+100A>T	NP_001243082.1:n.431+100A>T
NM_001320861.2:c.431+100A>T	NP_001307790.1:n.431+100A>T
NM_001320862.2:c.-5+100A>T	NP_001307791.1:n.-5+100A>T
NM_001256154.3:c.431+100A>T	NP_001243083.1:n.431+100A>T