Canonical Allele Identifier: CA8368301

Gene: ALOXE3

Linked Data

• dbSNP Id: rs780947567
• ExAC: 17:8015409 A / G
• gnomAD v2: 17-8015409-A-G
• gnomAD v4: 17-8112091-A-G
• MyVariant Identifiers: chr17:g.8015409A>G (hg19) ; chr17:g.8112091A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112091A>G , CM000679.2:g.8112091A>G	GRCh38
NC_000017.10:g.8015409A>G , CM000679.1:g.8015409A>G	GRCh37
NC_000017.9:g.7956134A>G	NCBI36
NG_015807.1:g.11826T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.784+2T>C	ENSP00000314879.4:n.784+2T>C
ENST00000380149.6:c.784+2T>C	ENSP00000369494.2:n.784+2T>C
ENST00000448843.7:c.784+2T>C MANE Select	ENSP00000400581.2:n.784+2T>C
ENST00000318227.3:c.1180+2T>C	ENSP00000314879.3:n.1180+2T>C
ENST00000380149.5:c.1252+2T>C	ENSP00000369494.1:n.1252+2T>C
ENST00000448843.6:c.784+2T>C	ENSP00000400581.2:n.784+2T>C
NM_001165960.1:c.1180+2T>C	NP_001159432.1:n.1180+2T>C
NM_021628.2:c.784+2T>C	NP_067641.2:n.784+2T>C
XM_017024921.2:c.784+2T>C	XP_016880410.1:n.784+2T>C
XM_017024922.2:c.784+2T>C	XP_016880411.1:n.784+2T>C
XM_017024923.2:c.784+2T>C	XP_016880412.1:n.784+2T>C
XM_017024924.2:c.784+2T>C	XP_016880413.1:n.784+2T>C
XM_017024925.2:c.784+2T>C	XP_016880414.1:n.784+2T>C
XR_001752579.2:n.1057+2T>C
XR_001752580.2:n.1057+2T>C
NM_001369446.1:c.781+2T>C	NP_001356375.1:n.781+2T>C
NM_021628.3:c.784+2T>C MANE Select	NP_067641.2:n.784+2T>C