Canonical Allele Identifier: CA397976489

Gene: ALOXE3

Linked Data

• MyVariant Identifiers: chr17:g.8015443T>G (hg19) ; chr17:g.8112125T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112125T>G , CM000679.2:g.8112125T>G	GRCh38
NC_000017.10:g.8015443T>G , CM000679.1:g.8015443T>G	GRCh37
NC_000017.9:g.7956168T>G	NCBI36
NG_015807.1:g.11792A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.752A>C	ENSP00000314879.4:p.Asn251Thr
ENST00000380149.6:c.752A>C	ENSP00000369494.2:p.Asn251Thr
ENST00000448843.7:c.752A>C MANE Select	ENSP00000400581.2:p.Asn251Thr
ENST00000318227.3:c.1148A>C	ENSP00000314879.3:p.Asn383Thr
ENST00000380149.5:c.1220A>C	ENSP00000369494.1:p.Asn407Thr
ENST00000448843.6:c.752A>C	ENSP00000400581.2:p.Asn251Thr
NM_001165960.1:c.1148A>C	NP_001159432.1:p.Asn383Thr
NM_021628.2:c.752A>C	NP_067641.2:p.Asn251Thr
XM_017024921.2:c.752A>C	XP_016880410.1:p.Asn251Thr
XM_017024922.2:c.752A>C	XP_016880411.1:p.Asn251Thr
XM_017024923.2:c.752A>C	XP_016880412.1:p.Asn251Thr
XM_017024924.2:c.752A>C	XP_016880413.1:p.Asn251Thr
XM_017024925.2:c.752A>C	XP_016880414.1:p.Asn251Thr
XR_001752579.2:n.1025A>C
XR_001752580.2:n.1025A>C
NM_001369446.1:c.749A>C	NP_001356375.1:p.Asn250Thr
NM_021628.3:c.752A>C MANE Select	NP_067641.2:p.Asn251Thr