Canonical Allele Identifier: CA772441982

Gene: ALOX15

Linked Data

• dbSNP Id: rs1404446299
• gnomAD v2: 17-4539446-A-G
• gnomAD v3: 17-4636151-A-G
• gnomAD v4: 17-4636151-A-G
• MyVariant Identifiers: chr17:g.4539446A>G (hg19) ; chr17:g.4636151A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636151A>G , CM000679.2:g.4636151A>G	GRCh38
NC_000017.10:g.4539446A>G , CM000679.1:g.4539446A>G	GRCh37
NC_000017.9:g.4486195A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-183T>C MANE Select	ENSP00000293761.3:n.952-183T>C
ENST00000570836.6:c.952-183T>C	ENSP00000458832.1:n.952-183T>C
ENST00000293761.7:c.952-183T>C	ENSP00000293761.3:n.952-183T>C
ENST00000570836.5:c.952-183T>C	ENSP00000458832.1:n.952-183T>C
ENST00000574640.1:c.835-183T>C	ENSP00000460483.1:n.835-183T>C
NM_001140.3:c.952-183T>C	NP_001131.3:n.952-183T>C
NM_001140.4:c.952-183T>C	NP_001131.3:n.952-183T>C
NM_001140.5:c.952-183T>C MANE Select	NP_001131.3:n.952-183T>C