Canonical Allele Identifier: CA2635535068
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631782-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631782G>C , CM000679.2:g.4631782G>C GRCh38
NC_000017.10:g.4535077G>C , CM000679.1:g.4535077G>C GRCh37
NC_000017.9:g.4481826G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1810-3C>G MANE Select ENSP00000293761.3:n.1810-3C>G
ENST00000570836.6:c.1810-3C>G ENSP00000458832.1:n.1810-3C>G
ENST00000293761.7:c.1810-3C>G ENSP00000293761.3:n.1810-3C>G
ENST00000570836.5:c.1810-3C>G ENSP00000458832.1:n.1810-3C>G
ENST00000574640.1:c.1693-3C>G ENSP00000460483.1:n.1693-3C>G
NM_001140.3:c.1810-3C>G NP_001131.3:n.1810-3C>G
NM_001140.4:c.1810-3C>G NP_001131.3:n.1810-3C>G
NM_001140.5:c.1810-3C>G MANE Select NP_001131.3:n.1810-3C>G