Canonical Allele Identifier: CA397246816
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535216T>C (hg19) chr17:g.4631921T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631921T>C , CM000679.2:g.4631921T>C GRCh38
NC_000017.10:g.4535216T>C , CM000679.1:g.4535216T>C GRCh37
NC_000017.9:g.4481965T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1777A>G MANE Select ENSP00000293761.3:p.Thr593Ala
ENST00000570836.6:c.1777A>G ENSP00000458832.1:p.Thr593Ala
ENST00000293761.7:c.1777A>G ENSP00000293761.3:p.Thr593Ala
ENST00000570836.5:c.1777A>G ENSP00000458832.1:p.Thr593Ala
ENST00000574640.1:c.1660A>G ENSP00000460483.1:p.Thr554Ala
NM_001140.3:c.1777A>G NP_001131.3:p.Thr593Ala
NM_001140.4:c.1777A>G NP_001131.3:p.Thr593Ala
NM_001140.5:c.1777A>G MANE Select NP_001131.3:p.Thr593Ala
Search 100 bp 5'
Search 100 bp 3'