Canonical Allele Identifier: CA397976756

Gene: ALOXE3

Linked Data

• MyVariant Identifiers: chr17:g.8015483C>A (hg19) ; chr17:g.8112165C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112165C>A , CM000679.2:g.8112165C>A	GRCh38
NC_000017.10:g.8015483C>A , CM000679.1:g.8015483C>A	GRCh37
NC_000017.9:g.7956208C>A	NCBI36
NG_015807.1:g.11752G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.712G>T	ENSP00000314879.4:p.Asp238Tyr
ENST00000380149.6:c.712G>T	ENSP00000369494.2:p.Asp238Tyr
ENST00000448843.7:c.712G>T MANE Select	ENSP00000400581.2:p.Asp238Tyr
ENST00000318227.3:c.1108G>T	ENSP00000314879.3:p.Asp370Tyr
ENST00000380149.5:c.1180G>T	ENSP00000369494.1:p.Asp394Tyr
ENST00000448843.6:c.712G>T	ENSP00000400581.2:p.Asp238Tyr
NM_001165960.1:c.1108G>T	NP_001159432.1:p.Asp370Tyr
NM_021628.2:c.712G>T	NP_067641.2:p.Asp238Tyr
XM_017024921.2:c.712G>T	XP_016880410.1:p.Asp238Tyr
XM_017024922.2:c.712G>T	XP_016880411.1:p.Asp238Tyr
XM_017024923.2:c.712G>T	XP_016880412.1:p.Asp238Tyr
XM_017024924.2:c.712G>T	XP_016880413.1:p.Asp238Tyr
XM_017024925.2:c.712G>T	XP_016880414.1:p.Asp238Tyr
XR_001752579.2:n.985G>T
XR_001752580.2:n.985G>T
NM_001369446.1:c.709G>T	NP_001356375.1:p.Asp237Tyr
NM_021628.3:c.712G>T MANE Select	NP_067641.2:p.Asp238Tyr