Canonical Allele Identifier: CA624854364

Gene: ALOX15

Linked Data

• dbSNP Id: rs1456449634
• gnomAD v2: 17-4534848-T-G
• gnomAD v3: 17-4631553-T-G
• gnomAD v4: 17-4631553-T-G
• MyVariant Identifiers: chr17:g.4534848T>G (hg19) ; chr17:g.4631553T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631553T>G , CM000679.2:g.4631553T>G	GRCh38
NC_000017.10:g.4534848T>G , CM000679.1:g.4534848T>G	GRCh37
NC_000017.9:g.4481597T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000293761.8:c.*47A>C MANE Select	ENSP00000293761.3:n.*47A>C
ENST00000570836.6:c.*47A>C	ENSP00000458832.1:n.*47A>C
ENST00000293761.7:c.*47A>C	ENSP00000293761.3:n.*47A>C
ENST00000570836.5:c.*47A>C	ENSP00000458832.1:n.*47A>C
ENST00000574640.1:c.*47A>C	ENSP00000460483.1:n.*47A>C
NM_001140.3:c.*47A>C	NP_001131.3:n.*47A>C
NM_001140.4:c.*47A>C	NP_001131.3:n.*47A>C
NM_001140.5:c.*47A>C MANE Select	NP_001131.3:n.*47A>C