Canonical Allele Identifier: CA8368304

Gene: ALOXE3

Linked Data

• ClinVar Variation Id: 888592
• ClinVar RCV Id: RCV001122020
• dbSNP Id: rs148293767
• ExAC: 17:8015415 C / T
• gnomAD v2: 17-8015415-C-T
• gnomAD v3: 17-8112097-C-T
• gnomAD v4: 17-8112097-C-T
• COSMIC: COSM242916
• MyVariant Identifiers: chr17:g.8015415C>T (hg19) ; chr17:g.8112097C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112097C>T , CM000679.2:g.8112097C>T	GRCh38
NC_000017.10:g.8015415C>T , CM000679.1:g.8015415C>T	GRCh37
NC_000017.9:g.7956140C>T	NCBI36
NG_015807.1:g.11820G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.780G>A	ENSP00000314879.4:p.Thr260=
ENST00000380149.6:c.780G>A	ENSP00000369494.2:p.Thr260=
ENST00000448843.7:c.780G>A MANE Select	ENSP00000400581.2:p.Thr260=
ENST00000318227.3:c.1176G>A	ENSP00000314879.3:p.Thr392=
ENST00000380149.5:c.1248G>A	ENSP00000369494.1:p.Thr416=
ENST00000448843.6:c.780G>A	ENSP00000400581.2:p.Thr260=
NM_001165960.1:c.1176G>A	NP_001159432.1:p.Thr392=
NM_021628.2:c.780G>A	NP_067641.2:p.Thr260=
XM_017024921.2:c.780G>A	XP_016880410.1:p.Thr260=
XM_017024922.2:c.780G>A	XP_016880411.1:p.Thr260=
XM_017024923.2:c.780G>A	XP_016880412.1:p.Thr260=
XM_017024924.2:c.780G>A	XP_016880413.1:p.Thr260=
XM_017024925.2:c.780G>A	XP_016880414.1:p.Thr260=
XR_001752579.2:n.1053G>A
XR_001752580.2:n.1053G>A
NM_001369446.1:c.777G>A	NP_001356375.1:p.Thr259=
NM_021628.3:c.780G>A MANE Select	NP_067641.2:p.Thr260=