Canonical Allele Identifier: CA624722359

Gene: ALOXE3

Linked Data

• dbSNP Id: rs1461101256
• gnomAD v2: 17-8015381-G-T
• gnomAD v4: 17-8112063-G-T
• MyVariant Identifiers: chr17:g.8015381G>T (hg19) ; chr17:g.8112063G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112063G>T , CM000679.2:g.8112063G>T	GRCh38
NC_000017.10:g.8015381G>T , CM000679.1:g.8015381G>T	GRCh37
NC_000017.9:g.7956106G>T	NCBI36
NG_015807.1:g.11854C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.784+30C>A	ENSP00000314879.4:n.784+30C>A
ENST00000380149.6:c.784+30C>A	ENSP00000369494.2:n.784+30C>A
ENST00000448843.7:c.784+30C>A MANE Select	ENSP00000400581.2:n.784+30C>A
ENST00000318227.3:c.1180+30C>A	ENSP00000314879.3:n.1180+30C>A
ENST00000380149.5:c.1252+30C>A	ENSP00000369494.1:n.1252+30C>A
ENST00000448843.6:c.784+30C>A	ENSP00000400581.2:n.784+30C>A
NM_001165960.1:c.1180+30C>A	NP_001159432.1:n.1180+30C>A
NM_021628.2:c.784+30C>A	NP_067641.2:n.784+30C>A
XM_017024921.2:c.784+30C>A	XP_016880410.1:n.784+30C>A
XM_017024922.2:c.784+30C>A	XP_016880411.1:n.784+30C>A
XM_017024923.2:c.784+30C>A	XP_016880412.1:n.784+30C>A
XM_017024924.2:c.784+30C>A	XP_016880413.1:n.784+30C>A
XM_017024925.2:c.784+30C>A	XP_016880414.1:n.784+30C>A
XR_001752579.2:n.1057+30C>A
XR_001752580.2:n.1057+30C>A
NM_001369446.1:c.781+30C>A	NP_001356375.1:n.781+30C>A
NM_021628.3:c.784+30C>A MANE Select	NP_067641.2:n.784+30C>A