Canonical Allele Identifier: CA397246986
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631966C>G , CM000679.2:g.4631966C>G GRCh38
NC_000017.10:g.4535261C>G , CM000679.1:g.4535261C>G GRCh37
NC_000017.9:g.4482010C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1732G>C MANE Select ENSP00000293761.3:p.Ala578Pro
ENST00000570836.6:c.1732G>C ENSP00000458832.1:p.Ala578Pro
ENST00000293761.7:c.1732G>C ENSP00000293761.3:p.Ala578Pro
ENST00000570836.5:c.1732G>C ENSP00000458832.1:p.Ala578Pro
ENST00000574640.1:c.1615G>C ENSP00000460483.1:p.Ala539Pro
NM_001140.3:c.1732G>C NP_001131.3:p.Ala578Pro
NM_001140.4:c.1732G>C NP_001131.3:p.Ala578Pro
NM_001140.5:c.1732G>C MANE Select NP_001131.3:p.Ala578Pro