Canonical Allele Identifier: CA287524520

Gene: ALOXE3

Linked Data

• ClinVar Variation Id: 890817
• ClinVar RCV Id: RCV001125693
• dbSNP Id: rs963782279
• MyVariant Identifiers: chr17:g.8011835G>A (hg19) ; chr17:g.8108517G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8108517G>A , CM000679.2:g.8108517G>A	GRCh38
NC_000017.10:g.8011835G>A , CM000679.1:g.8011835G>A	GRCh37
NC_000017.9:g.7952560G>A	NCBI36
NG_015807.1:g.15400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.1635C>T	ENSP00000314879.4:p.Ala545=
ENST00000380149.6:c.1635C>T	ENSP00000369494.2:p.Ala545=
ENST00000448843.7:c.1635C>T MANE Select	ENSP00000400581.2:p.Ala545=
ENST00000318227.3:c.2031C>T	ENSP00000314879.3:p.Ala677=
ENST00000380149.5:c.2103C>T	ENSP00000369494.1:p.Ala701=
ENST00000448843.6:c.1635C>T	ENSP00000400581.2:p.Ala545=
NM_001165960.1:c.2031C>T	NP_001159432.1:p.Ala677=
NM_021628.2:c.1635C>T	NP_067641.2:p.Ala545=
XM_017024921.2:c.1635C>T	XP_016880410.1:p.Ala545=
XM_017024922.2:c.1562+657C>T	XP_016880411.1:n.1562+657C>T
XM_017024924.2:c.*76C>T	XP_016880413.1:n.*76C>T
XR_001752579.2:n.1835+657C>T
XR_001752580.2:n.1746+657C>T
NM_001369446.1:c.1632C>T	NP_001356375.1:p.Ala544=
NM_021628.3:c.1635C>T MANE Select	NP_067641.2:p.Ala545=