Canonical Allele Identifier: CA1772845204

Gene: EPHX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27500915G= , CM000670.2:g.27500915G=	GRCh38
NC_000008.10:g.27358432G= , CM000670.1:g.27358432G=	GRCh37
NC_000008.9:g.27414349G=	NCBI36
NG_012064.1:g.14788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.102-11G= MANE Select	ENSP00000430269.1:n.102-11G=
ENST00000380476.7:c.-20-49G=	ENSP00000369843.3:n.-20-49G=
ENST00000517536.5:c.102-11G=	ENSP00000428875.1:n.102-11G=
ENST00000518328.5:c.102-11G=	ENSP00000430779.1:n.102-11G=
ENST00000518379.5:c.102-11G=	ENSP00000427956.1:n.102-11G=
ENST00000520623.5:n.186-11G=
ENST00000520666.1:n.116-13G=
ENST00000521400.5:c.102-11G=	ENSP00000430269.1:n.102-11G=
ENST00000521684.1:c.101-11G=
ENST00000521780.5:c.-12-2689G=	ENSP00000430302.1:n.-12-2689G=
ENST00000523827.1:n.325-11G=
NM_001256482.1:c.-20-49G=	NP_001243411.1:n.-20-49G=
NM_001256483.1:c.-12-2689G=	NP_001243412.1:n.-12-2689G=
NM_001256484.1:c.-56-13G=	NP_001243413.1:n.-56-13G=
NM_001979.5:c.102-11G=	NP_001970.2:n.102-11G=
XM_017013199.1:c.102-11G=	XP_016868688.1:n.102-11G=
XM_017013200.1:c.102-11G=	XP_016868689.1:n.102-11G=
XR_001745491.1:n.160-11G=
NM_001256482.2:c.-20-49G=	NP_001243411.1:n.-20-49G=
NM_001256483.2:c.-12-2689G=	NP_001243412.1:n.-12-2689G=
NM_001256484.2:c.-56-13G=	NP_001243413.1:n.-56-13G=
NM_001979.6:c.102-11G= MANE Select	NP_001970.2:n.102-11G=