Canonical Allele Identifier: CA13220078
Gene: ALOX5 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.45396036A>G
GRCh37 chr10:g.45891484A>G
gnomAD v2:
10:45891484 A / G
gnomAD v3:
10:45396036 A / G
gnomAD v4:
chr10-45396036-A-G
Joint Max Group AF 0.59238079 (EAS)
Genomes Max Group AF 0.58887409 (EAS)
Exomes Max Group AF 0.59071408 (EAS)
dbSNP:
2029253
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Genomic Alleles

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

Transcript Alleles

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