Canonical Allele Identifier: CA397246965
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631960G>C , CM000679.2:g.4631960G>C GRCh38
NC_000017.10:g.4535255G>C , CM000679.1:g.4535255G>C GRCh37
NC_000017.9:g.4482004G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1738C>G MANE Select ENSP00000293761.3:p.Leu580Val
ENST00000570836.6:c.1738C>G ENSP00000458832.1:p.Leu580Val
ENST00000293761.7:c.1738C>G ENSP00000293761.3:p.Leu580Val
ENST00000570836.5:c.1738C>G ENSP00000458832.1:p.Leu580Val
ENST00000574640.1:c.1621C>G ENSP00000460483.1:p.Leu541Val
NM_001140.3:c.1738C>G NP_001131.3:p.Leu580Val
NM_001140.4:c.1738C>G NP_001131.3:p.Leu580Val
NM_001140.5:c.1738C>G MANE Select NP_001131.3:p.Leu580Val