Canonical Allele Identifier: CA1772863130

Gene: EPHX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27516348G= , CM000670.2:g.27516348G=	GRCh38
NC_000008.10:g.27373865G= , CM000670.1:g.27373865G=	GRCh37
NC_000008.9:g.27429782G=	NCBI36
NG_012064.1:g.30221G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.860G= MANE Select	ENSP00000430269.1:p.Arg287=
ENST00000380476.7:c.701G=	ENSP00000369843.3:p.Arg234=
ENST00000517536.5:c.311G=	ENSP00000428875.1:p.Arg104=
ENST00000518379.5:c.764G=	ENSP00000427956.1:p.Arg255=
ENST00000520623.5:n.944G=
ENST00000521400.5:c.860G=	ENSP00000430269.1:p.Arg287=
ENST00000521684.1:c.736G=
ENST00000521780.5:c.662G=	ENSP00000430302.1:p.Arg221=
ENST00000523326.1:n.380G=
NM_001256482.1:c.701G=	NP_001243411.1:p.Arg234=
NM_001256483.1:c.662G=	NP_001243412.1:p.Arg221=
NM_001256484.1:c.701G=	NP_001243413.1:p.Arg234=
NM_001979.5:c.860G=	NP_001970.2:p.Arg287=
XM_017013199.1:c.737G=	XP_016868688.1:p.Arg246=
XR_001745491.1:n.918G=
NM_001256482.2:c.701G=	NP_001243411.1:p.Arg234=
NM_001256483.2:c.662G=	NP_001243412.1:p.Arg221=
NM_001256484.2:c.701G=	NP_001243413.1:p.Arg234=
NM_001979.6:c.860G= MANE Select	NP_001970.2:p.Arg287=