Canonical Allele Identifier: CA1772845365

Gene: EPHX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27500988A= , CM000670.2:g.27500988A=	GRCh38
NC_000008.10:g.27358505A= , CM000670.1:g.27358505A=	GRCh37
NC_000008.9:g.27414422A=	NCBI36
NG_012064.1:g.14861A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001979.6:c.164A= MANE Select	NP_001970.2:p.Lys55=
ENST00000521400.6:c.164A= MANE Select	ENSP00000430269.1:p.Lys55=
NM_001256482.1:c.5A=	NP_001243411.1:p.Lys2=
NM_001256482.2:c.5A=	NP_001243411.1:p.Lys2=
NM_001256483.1:c.-12-2616A=	NP_001243412.1:n.-12-2616A=
NM_001256483.2:c.-12-2616A=	NP_001243412.1:n.-12-2616A=
NM_001256484.1:c.5A=	NP_001243413.1:p.Lys2=
NM_001256484.2:c.5A=	NP_001243413.1:p.Lys2=
NM_001979.5:c.164A=	NP_001970.2:p.Lys55=
ENST00000380476.7:c.5A=	ENSP00000369843.3:p.Lys2=
ENST00000517536.5:c.164A=	ENSP00000428875.1:p.Lys55=
ENST00000518328.5:c.164A=	ENSP00000430779.1:p.Lys55=
ENST00000518379.5:c.164A=	ENSP00000427956.1:p.Lys55=
ENST00000520623.5:n.248A=
ENST00000520666.1:n.176A=
ENST00000521400.5:c.164A=	ENSP00000430269.1:p.Lys55=
ENST00000521684.1:c.163A=
ENST00000521780.5:c.-12-2616A=	ENSP00000430302.1:n.-12-2616A=
ENST00000523827.1:n.387A=
XM_017013199.1:c.164A=	XP_016868688.1:p.Lys55=
XM_017013200.1:c.164A=	XP_016868689.1:p.Lys55=
XR_001745491.1:n.222A=