Canonical Allele Identifier: CA469074474

Gene: ALOX5

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.45382602G>C , CM000672.2:g.45382602G>C	GRCh38
NC_000010.10:g.45878050G>C , CM000672.1:g.45878050G>C	GRCh37
NC_000010.9:g.45198056G>C	NCBI36
NG_011437.1:g.13422G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000698.5:c.270G>C MANE Select	NP_000689.1:p.Thr90=
ENST00000374391.7:c.270G>C MANE Select	ENSP00000363512.2:p.Thr90=
NM_000698.3:c.270G>C	NP_000689.1:p.Thr90=
NM_000698.4:c.270G>C	NP_000689.1:p.Thr90=
NM_001256153.1:c.270G>C	NP_001243082.1:p.Thr90=
NM_001256153.2:c.270G>C	NP_001243082.1:p.Thr90=
NM_001256153.3:c.270G>C	NP_001243082.1:p.Thr90=
NM_001256154.1:c.270G>C	NP_001243083.1:p.Thr90=
NM_001256154.2:c.270G>C	NP_001243083.1:p.Thr90=
NM_001256154.3:c.270G>C	NP_001243083.1:p.Thr90=
NM_001320861.1:c.270G>C	NP_001307790.1:p.Thr90=
NM_001320861.2:c.270G>C	NP_001307790.1:p.Thr90=
NM_001320862.1:c.-166G>C	NP_001307791.1:n.-166G>C
NM_001320862.2:c.-166G>C	NP_001307791.1:n.-166G>C
ENST00000374391.6:c.270G>C	ENSP00000363512.2:p.Thr90=
ENST00000542434.5:c.270G>C	ENSP00000437634.1:p.Thr90=
ENST00000612635.4:c.270G>C	ENSP00000483803.1:p.Thr90=
XM_011539564.1:c.270G>C	XP_011537866.1:p.Thr90=
XM_017016012.1:c.-84G>C	XP_016871501.1:n.-84G>C
XR_001747075.1:n.337G>C