Canonical Allele Identifier: CA497752025

Gene: ALOXE3

Linked Data

• MyVariant Identifiers: chr17:g.8015511G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112193G>C , CM000679.2:g.8112193G>C	GRCh38
NC_000017.10:g.8015511G>C , CM000679.1:g.8015511G>C	GRCh37
NC_000017.9:g.7956236G>C	NCBI36
NG_015807.1:g.11724C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.684C>G	ENSP00000314879.4:p.Ser228=
ENST00000380149.6:c.684C>G	ENSP00000369494.2:p.Ser228=
ENST00000448843.7:c.684C>G MANE Select	ENSP00000400581.2:p.Ser228=
ENST00000318227.3:c.1080C>G	ENSP00000314879.3:p.Ser360=
ENST00000380149.5:c.1152C>G	ENSP00000369494.1:p.Ser384=
ENST00000448843.6:c.684C>G	ENSP00000400581.2:p.Ser228=
NM_001165960.1:c.1080C>G	NP_001159432.1:p.Ser360=
NM_021628.2:c.684C>G	NP_067641.2:p.Ser228=
XM_017024921.2:c.684C>G	XP_016880410.1:p.Ser228=
XM_017024922.2:c.684C>G	XP_016880411.1:p.Ser228=
XM_017024923.2:c.684C>G	XP_016880412.1:p.Ser228=
XM_017024924.2:c.684C>G	XP_016880413.1:p.Ser228=
XM_017024925.2:c.684C>G	XP_016880414.1:p.Ser228=
XR_001752579.2:n.957C>G
XR_001752580.2:n.957C>G
NM_001369446.1:c.681C>G	NP_001356375.1:p.Ser227=
NM_021628.3:c.684C>G MANE Select	NP_067641.2:p.Ser228=