Canonical Allele Identifier: CA397246973
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535258T>A (hg19) chr17:g.4631963T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631963T>A , CM000679.2:g.4631963T>A GRCh38
NC_000017.10:g.4535258T>A , CM000679.1:g.4535258T>A GRCh37
NC_000017.9:g.4482007T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1735A>T MANE Select ENSP00000293761.3:p.Thr579Ser
ENST00000570836.6:c.1735A>T ENSP00000458832.1:p.Thr579Ser
ENST00000293761.7:c.1735A>T ENSP00000293761.3:p.Thr579Ser
ENST00000570836.5:c.1735A>T ENSP00000458832.1:p.Thr579Ser
ENST00000574640.1:c.1618A>T ENSP00000460483.1:p.Thr540Ser
NM_001140.3:c.1735A>T NP_001131.3:p.Thr579Ser
NM_001140.4:c.1735A>T NP_001131.3:p.Thr579Ser
NM_001140.5:c.1735A>T MANE Select NP_001131.3:p.Thr579Ser
Search 100 bp 5'
Search 100 bp 3'