Canonical Allele Identifier: CA8368032

Gene: ALOXE3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8108591T>C , CM000679.2:g.8108591T>C	GRCh38
NC_000017.10:g.8011909T>C , CM000679.1:g.8011909T>C	GRCh37
NC_000017.9:g.7952634T>C	NCBI36
NG_015807.1:g.15326A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021628.3:c.1563-2A>G MANE Select	NP_067641.2:n.1563-2A>G
ENST00000448843.7:c.1563-2A>G MANE Select	ENSP00000400581.2:n.1563-2A>G
NM_001165960.1:c.1959-2A>G	NP_001159432.1:n.1959-2A>G
NM_001369446.1:c.1560-2A>G	NP_001356375.1:n.1560-2A>G
NM_021628.2:c.1563-2A>G	NP_067641.2:n.1563-2A>G
ENST00000318227.3:c.1959-2A>G	ENSP00000314879.3:n.1959-2A>G
ENST00000318227.4:c.1563-2A>G	ENSP00000314879.4:n.1563-2A>G
ENST00000380149.5:c.2031-2A>G	ENSP00000369494.1:n.2031-2A>G
ENST00000380149.6:c.1563-2A>G	ENSP00000369494.2:n.1563-2A>G
ENST00000448843.6:c.1563-2A>G	ENSP00000400581.2:n.1563-2A>G
XM_017024921.2:c.1563-2A>G	XP_016880410.1:n.1563-2A>G
XM_017024922.2:c.1562+583A>G	XP_016880411.1:n.1562+583A>G
XM_017024924.2:c.*4-2A>G	XP_016880413.1:n.*4-2A>G
XR_001752579.2:n.1835+583A>G
XR_001752580.2:n.1746+583A>G