Canonical Allele Identifier: CA397247029
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535271C>A (hg19) chr17:g.4631976C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631976C>A , CM000679.2:g.4631976C>A GRCh38
NC_000017.10:g.4535271C>A , CM000679.1:g.4535271C>A GRCh37
NC_000017.9:g.4482020C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1722G>T MANE Select ENSP00000293761.3:p.Glu574Asp
ENST00000570836.6:c.1722G>T ENSP00000458832.1:p.Glu574Asp
ENST00000293761.7:c.1722G>T ENSP00000293761.3:p.Glu574Asp
ENST00000570836.5:c.1722G>T ENSP00000458832.1:p.Glu574Asp
ENST00000574640.1:c.1605G>T ENSP00000460483.1:p.Glu535Asp
NM_001140.3:c.1722G>T NP_001131.3:p.Glu574Asp
NM_001140.4:c.1722G>T NP_001131.3:p.Glu574Asp
NM_001140.5:c.1722G>T MANE Select NP_001131.3:p.Glu574Asp
Search 100 bp 5'
Search 100 bp 3'