Canonical Allele Identifier: CA397246730

Gene: ALOX15

Linked Data

• dbSNP Id: rs141061806
• gnomAD v2: 17-4535189-C-A
• MyVariant Identifiers: chr17:g.4535189C>A (hg19) ; chr17:g.4631894C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631894C>A , CM000679.2:g.4631894C>A	GRCh38
NC_000017.10:g.4535189C>A , CM000679.1:g.4535189C>A	GRCh37
NC_000017.9:g.4481938C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1804G>T MANE Select	ENSP00000293761.3:p.Val602Phe
ENST00000570836.6:c.1804G>T	ENSP00000458832.1:p.Val602Phe
ENST00000293761.7:c.1804G>T	ENSP00000293761.3:p.Val602Phe
ENST00000570836.5:c.1804G>T	ENSP00000458832.1:p.Val602Phe
ENST00000574640.1:c.1687G>T	ENSP00000460483.1:p.Val563Phe
NM_001140.3:c.1804G>T	NP_001131.3:p.Val602Phe
NM_001140.4:c.1804G>T	NP_001131.3:p.Val602Phe
NM_001140.5:c.1804G>T MANE Select	NP_001131.3:p.Val602Phe