Canonical Allele Identifier: CA10650442

Gene: ALOXE3

Linked Data

• ClinVar Variation Id: 325951
• ClinVar RCV Id: RCV000324541
• dbSNP Id: rs886053583
• MyVariant Identifiers: chr17:g.7999723G>C (hg19) ; chr17:g.8096405G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8096405G>C , CM000679.2:g.8096405G>C	GRCh38
NC_000017.10:g.7999723G>C , CM000679.1:g.7999723G>C	GRCh37
NC_000017.9:g.7940448G>C	NCBI36
NG_015807.1:g.27512C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.*222C>G	ENSP00000314879.4:n.*222C>G
ENST00000380149.6:c.*222C>G	ENSP00000369494.2:n.*222C>G
ENST00000448843.7:c.*222C>G MANE Select	ENSP00000400581.2:n.*222C>G
ENST00000318227.3:c.*222C>G	ENSP00000314879.3:n.*222C>G
ENST00000380149.5:c.*222C>G	ENSP00000369494.1:n.*222C>G
ENST00000448843.6:c.*222C>G	ENSP00000400581.2:n.*222C>G
ENST00000583808.1:n.595C>G
NM_001165960.1:c.*222C>G	NP_001159432.1:n.*222C>G
NM_021628.2:c.*222C>G	NP_067641.2:n.*222C>G
XR_001752579.2:n.2509C>G
NM_001369446.1:c.*222C>G	NP_001356375.1:n.*222C>G
NM_021628.3:c.*222C>G MANE Select	NP_067641.2:n.*222C>G