Canonical Allele Identifier: CA14393604
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs916055
gnomAD v2: 17-4534834-A-G
gnomAD v3: 17-4631539-A-G
gnomAD v4: 17-4631539-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631539A>G , CM000679.2:g.4631539A>G GRCh38
NC_000017.10:g.4534834A>G , CM000679.1:g.4534834A>G GRCh37
NC_000017.9:g.4481583A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*61T>C MANE Select ENSP00000293761.3:n.*61T>C
ENST00000570836.6:c.*61T>C ENSP00000458832.1:n.*61T>C
ENST00000293761.7:c.*61T>C ENSP00000293761.3:n.*61T>C
ENST00000570836.5:c.*61T>C ENSP00000458832.1:n.*61T>C
ENST00000574640.1:c.*61T>C ENSP00000460483.1:n.*61T>C
NM_001140.3:c.*61T>C NP_001131.3:n.*61T>C
NM_001140.4:c.*61T>C NP_001131.3:n.*61T>C
NM_001140.5:c.*61T>C MANE Select NP_001131.3:n.*61T>C