Canonical Allele Identifier: CA397246966
Gene: ALOX15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4535255G>T (hg19) chr17:g.4631960G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631960G>T , CM000679.2:g.4631960G>T GRCh38
NC_000017.10:g.4535255G>T , CM000679.1:g.4535255G>T GRCh37
NC_000017.9:g.4482004G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1738C>A MANE Select ENSP00000293761.3:p.Leu580Met
ENST00000570836.6:c.1738C>A ENSP00000458832.1:p.Leu580Met
ENST00000293761.7:c.1738C>A ENSP00000293761.3:p.Leu580Met
ENST00000570836.5:c.1738C>A ENSP00000458832.1:p.Leu580Met
ENST00000574640.1:c.1621C>A ENSP00000460483.1:p.Leu541Met
NM_001140.3:c.1738C>A NP_001131.3:p.Leu580Met
NM_001140.4:c.1738C>A NP_001131.3:p.Leu580Met
NM_001140.5:c.1738C>A MANE Select NP_001131.3:p.Leu580Met
Search 100 bp 5'
Search 100 bp 3'