Canonical Allele Identifier: CA397246931
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535247G>C (hg19) chr17:g.4631952G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631952G>C , CM000679.2:g.4631952G>C GRCh38
NC_000017.10:g.4535247G>C , CM000679.1:g.4535247G>C GRCh37
NC_000017.9:g.4481996G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1746C>G MANE Select ENSP00000293761.3:p.Asn582Lys
ENST00000570836.6:c.1746C>G ENSP00000458832.1:p.Asn582Lys
ENST00000293761.7:c.1746C>G ENSP00000293761.3:p.Asn582Lys
ENST00000570836.5:c.1746C>G ENSP00000458832.1:p.Asn582Lys
ENST00000574640.1:c.1629C>G ENSP00000460483.1:p.Asn543Lys
NM_001140.3:c.1746C>G NP_001131.3:p.Asn582Lys
NM_001140.4:c.1746C>G NP_001131.3:p.Asn582Lys
NM_001140.5:c.1746C>G MANE Select NP_001131.3:p.Asn582Lys
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