Canonical Allele Identifier: CA287132914

Gene: ALOX15

Linked Data

• dbSNP Id: rs951324992
• gnomAD v3: 17-4631515-A-G
• gnomAD v4: 17-4631515-A-G
• MyVariant Identifiers: chr17:g.4534810A>G (hg19) ; chr17:g.4631515A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631515A>G , CM000679.2:g.4631515A>G	GRCh38
NC_000017.10:g.4534810A>G , CM000679.1:g.4534810A>G	GRCh37
NC_000017.9:g.4481559A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*85T>C MANE Select	ENSP00000293761.3:n.*85T>C
ENST00000570836.6:c.*85T>C	ENSP00000458832.1:n.*85T>C
ENST00000293761.7:c.*85T>C	ENSP00000293761.3:n.*85T>C
ENST00000570836.5:c.*85T>C	ENSP00000458832.1:n.*85T>C
ENST00000574640.1:c.*85T>C	ENSP00000460483.1:n.*85T>C
NM_001140.3:c.*85T>C	NP_001131.3:n.*85T>C
NM_001140.4:c.*85T>C	NP_001131.3:n.*85T>C
NM_001140.5:c.*85T>C MANE Select	NP_001131.3:n.*85T>C