Canonical Allele Identifier: CA8306683
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs746860191
gnomAD v2: 17-4535210-G-T
gnomAD v3: 17-4631915-G-T
gnomAD v4: 17-4631915-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631915G>T , CM000679.2:g.4631915G>T GRCh38
NC_000017.10:g.4535210G>T , CM000679.1:g.4535210G>T GRCh37
NC_000017.9:g.4481959G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1783C>A MANE Select ENSP00000293761.3:p.Gln595Lys
ENST00000570836.6:c.1783C>A ENSP00000458832.1:p.Gln595Lys
ENST00000293761.7:c.1783C>A ENSP00000293761.3:p.Gln595Lys
ENST00000570836.5:c.1783C>A ENSP00000458832.1:p.Gln595Lys
ENST00000574640.1:c.1666C>A ENSP00000460483.1:p.Gln556Lys
NM_001140.3:c.1783C>A NP_001131.3:p.Gln595Lys
NM_001140.4:c.1783C>A NP_001131.3:p.Gln595Lys
NM_001140.5:c.1783C>A MANE Select NP_001131.3:p.Gln595Lys