Canonical Allele Identifier: CA665554878

Gene: ALOX5

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.45421928C>G , CM000672.2:g.45421928C>G	GRCh38
NC_000010.10:g.45917376C>G , CM000672.1:g.45917376C>G	GRCh37
NC_000010.9:g.45237382C>G	NCBI36
NG_011437.1:g.52748C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374391.7:c.555-2113C>G MANE Select	ENSP00000363512.2:n.555-2113C>G
ENST00000374391.6:c.555-2113C>G	ENSP00000363512.2:n.555-2113C>G
ENST00000542434.5:c.555-2113C>G	ENSP00000437634.1:n.555-2113C>G
ENST00000612635.4:c.475-2113C>G	ENSP00000483803.1:n.475-2113C>G
NM_000698.3:c.555-2113C>G	NP_000689.1:n.555-2113C>G
NM_001256153.1:c.555-2113C>G	NP_001243082.1:n.555-2113C>G
NM_001256154.1:c.555-2113C>G	NP_001243083.1:n.555-2113C>G
XM_011539564.1:c.555-2113C>G	XP_011537866.1:n.555-2113C>G
NM_000698.4:c.555-2113C>G	NP_000689.1:n.555-2113C>G
NM_001256153.2:c.555-2113C>G	NP_001243082.1:n.555-2113C>G
NM_001256154.2:c.555-2113C>G	NP_001243083.1:n.555-2113C>G
NM_001320861.1:c.555-2113C>G	NP_001307790.1:n.555-2113C>G
NM_001320862.1:c.120-2113C>G	NP_001307791.1:n.120-2113C>G
XM_017016012.1:c.120-2113C>G	XP_016871501.1:n.120-2113C>G
XR_001747075.1:n.622-2113C>G
NM_000698.5:c.555-2113C>G MANE Select	NP_000689.1:n.555-2113C>G
NM_001256153.3:c.555-2113C>G	NP_001243082.1:n.555-2113C>G
NM_001320861.2:c.555-2113C>G	NP_001307790.1:n.555-2113C>G
NM_001320862.2:c.120-2113C>G	NP_001307791.1:n.120-2113C>G
NM_001256154.3:c.555-2113C>G	NP_001243083.1:n.555-2113C>G