Canonical Allele Identifier: CA1772845220

Gene: EPHX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27500930C= , CM000670.2:g.27500930C=	GRCh38
NC_000008.10:g.27358447C= , CM000670.1:g.27358447C=	GRCh37
NC_000008.9:g.27414364C=	NCBI36
NG_012064.1:g.14803C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.106C= MANE Select	ENSP00000430269.1:p.Leu36=
ENST00000380476.7:c.-20-34C=	ENSP00000369843.3:n.-20-34C=
ENST00000517536.5:c.106C=	ENSP00000428875.1:p.Leu36=
ENST00000518328.5:c.106C=	ENSP00000430779.1:p.Leu36=
ENST00000518379.5:c.106C=	ENSP00000427956.1:p.Leu36=
ENST00000520623.5:n.190C=
ENST00000520666.1:n.118C=
ENST00000521400.5:c.106C=	ENSP00000430269.1:p.Leu36=
ENST00000521684.1:c.105C=
ENST00000521780.5:c.-12-2674C=	ENSP00000430302.1:n.-12-2674C=
ENST00000523827.1:n.329C=
NM_001256482.1:c.-20-34C=	NP_001243411.1:n.-20-34C=
NM_001256483.1:c.-12-2674C=	NP_001243412.1:n.-12-2674C=
NM_001256484.1:c.-54C=	NP_001243413.1:n.-54C=
NM_001979.5:c.106C=	NP_001970.2:p.Leu36=
XM_017013199.1:c.106C=	XP_016868688.1:p.Leu36=
XM_017013200.1:c.106C=	XP_016868689.1:p.Leu36=
XR_001745491.1:n.164C=
NM_001256482.2:c.-20-34C=	NP_001243411.1:n.-20-34C=
NM_001256483.2:c.-12-2674C=	NP_001243412.1:n.-12-2674C=
NM_001256484.2:c.-54C=	NP_001243413.1:n.-54C=
NM_001979.6:c.106C= MANE Select	NP_001970.2:p.Leu36=