Canonical Allele Identifier: CA397976724

Gene: ALOXE3

Linked Data

• dbSNP Id: rs141814242
• gnomAD v3: 17-8112161-C-G
• gnomAD v4: 17-8112161-C-G
• MyVariant Identifiers: chr17:g.8015479C>G (hg19) ; chr17:g.8112161C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112161C>G , CM000679.2:g.8112161C>G	GRCh38
NC_000017.10:g.8015479C>G , CM000679.1:g.8015479C>G	GRCh37
NC_000017.9:g.7956204C>G	NCBI36
NG_015807.1:g.11756G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.716G>C	ENSP00000314879.4:p.Arg239Pro
ENST00000380149.6:c.716G>C	ENSP00000369494.2:p.Arg239Pro
ENST00000448843.7:c.716G>C MANE Select	ENSP00000400581.2:p.Arg239Pro
ENST00000318227.3:c.1112G>C	ENSP00000314879.3:p.Arg371Pro
ENST00000380149.5:c.1184G>C	ENSP00000369494.1:p.Arg395Pro
ENST00000448843.6:c.716G>C	ENSP00000400581.2:p.Arg239Pro
NM_001165960.1:c.1112G>C	NP_001159432.1:p.Arg371Pro
NM_021628.2:c.716G>C	NP_067641.2:p.Arg239Pro
XM_017024921.2:c.716G>C	XP_016880410.1:p.Arg239Pro
XM_017024922.2:c.716G>C	XP_016880411.1:p.Arg239Pro
XM_017024923.2:c.716G>C	XP_016880412.1:p.Arg239Pro
XM_017024924.2:c.716G>C	XP_016880413.1:p.Arg239Pro
XM_017024925.2:c.716G>C	XP_016880414.1:p.Arg239Pro
XR_001752579.2:n.989G>C
XR_001752580.2:n.989G>C
NM_001369446.1:c.713G>C	NP_001356375.1:p.Arg238Pro
NM_021628.3:c.716G>C MANE Select	NP_067641.2:p.Arg239Pro