Canonical Allele Identifier: CA772437789
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1183287456
gnomAD v3: 17-4631761-C-CA
gnomAD v4: 17-4631761-C-CA
MyVariant Identifiers: chr17:g.4535056_4535057insA (hg19) chr17:g.4631761_4631762insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631762dup , CM000679.2:g.4631762dup GRCh38
NC_000017.10:g.4535057dup , CM000679.1:g.4535057dup GRCh37
NC_000017.9:g.4481806dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1827dup MANE Select ENSP00000293761.3:p.Glu610Ter
ENST00000570836.6:c.1827dup ENSP00000458832.1:p.Glu610Ter
ENST00000293761.7:c.1827dup ENSP00000293761.3:p.Glu610Ter
ENST00000570836.5:c.1827dup ENSP00000458832.1:p.Glu610Ter
ENST00000574640.1:c.1710dup ENSP00000460483.1:p.Glu571Ter
NM_001140.3:c.1827dup NP_001131.3:p.Glu610Ter
NM_001140.4:c.1827dup NP_001131.3:p.Glu610Ter
NM_001140.5:c.1827dup MANE Select NP_001131.3:p.Glu610Ter
Search 100 bp 5'
Search 100 bp 3'