Canonical Allele Identifier: CA1772845244

Gene: EPHX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27500940A= , CM000670.2:g.27500940A=	GRCh38
NC_000008.10:g.27358457A= , CM000670.1:g.27358457A=	GRCh37
NC_000008.9:g.27414374A=	NCBI36
NG_012064.1:g.14813A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.116A= MANE Select	ENSP00000430269.1:p.Asp39=
ENST00000380476.7:c.-20-24A=	ENSP00000369843.3:n.-20-24A=
ENST00000517536.5:c.116A=	ENSP00000428875.1:p.Asp39=
ENST00000518328.5:c.116A=	ENSP00000430779.1:p.Asp39=
ENST00000518379.5:c.116A=	ENSP00000427956.1:p.Asp39=
ENST00000520623.5:n.200A=
ENST00000520666.1:n.128A=
ENST00000521400.5:c.116A=	ENSP00000430269.1:p.Asp39=
ENST00000521684.1:c.115A=
ENST00000521780.5:c.-12-2664A=	ENSP00000430302.1:n.-12-2664A=
ENST00000523827.1:n.339A=
NM_001256482.1:c.-20-24A=	NP_001243411.1:n.-20-24A=
NM_001256483.1:c.-12-2664A=	NP_001243412.1:n.-12-2664A=
NM_001256484.1:c.-44A=	NP_001243413.1:n.-44A=
NM_001979.5:c.116A=	NP_001970.2:p.Asp39=
XM_017013199.1:c.116A=	XP_016868688.1:p.Asp39=
XM_017013200.1:c.116A=	XP_016868689.1:p.Asp39=
XR_001745491.1:n.174A=
NM_001256482.2:c.-20-24A=	NP_001243411.1:n.-20-24A=
NM_001256483.2:c.-12-2664A=	NP_001243412.1:n.-12-2664A=
NM_001256484.2:c.-44A=	NP_001243413.1:n.-44A=
NM_001979.6:c.116A= MANE Select	NP_001970.2:p.Asp39=