Canonical Allele Identifier: CA1772845154

Gene: EPHX2

Linked Data

• dbSNP Id: rs1813739637

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27500874_27500875del , CM000670.2:g.27500874_27500875del	GRCh38
NC_000008.10:g.27358391_27358392del , CM000670.1:g.27358391_27358392del	GRCh37
NC_000008.9:g.27414308_27414309del	NCBI36
NG_012064.1:g.14747_14748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.102-52_102-51del MANE Select	ENSP00000430269.1:n.102-52_102-51del
ENST00000380476.7:c.-20-90_-20-89del	ENSP00000369843.3:n.-20-90_-20-89del
ENST00000517536.5:c.102-52_102-51del	ENSP00000428875.1:n.102-52_102-51del
ENST00000518328.5:c.102-52_102-51del	ENSP00000430779.1:n.102-52_102-51del
ENST00000518379.5:c.102-52_102-51del	ENSP00000427956.1:n.102-52_102-51del
ENST00000520623.5:n.186-52_186-51del
ENST00000520666.1:n.116-54_116-53del
ENST00000521400.5:c.102-52_102-51del	ENSP00000430269.1:n.102-52_102-51del
ENST00000521684.1:c.101-52_101-51del
ENST00000521780.5:c.-12-2730_-12-2729del	ENSP00000430302.1:n.-12-2730_-12-2729del
ENST00000523827.1:n.325-52_325-51del
NM_001256482.1:c.-20-90_-20-89del	NP_001243411.1:n.-20-90_-20-89del
NM_001256483.1:c.-12-2730_-12-2729del	NP_001243412.1:n.-12-2730_-12-2729del
NM_001256484.1:c.-56-54_-56-53del	NP_001243413.1:n.-56-54_-56-53del
NM_001979.5:c.102-52_102-51del	NP_001970.2:n.102-52_102-51del
XM_017013199.1:c.102-52_102-51del	XP_016868688.1:n.102-52_102-51del
XM_017013200.1:c.102-52_102-51del	XP_016868689.1:n.102-52_102-51del
XR_001745491.1:n.160-52_160-51del
NM_001256482.2:c.-20-90_-20-89del	NP_001243411.1:n.-20-90_-20-89del
NM_001256483.2:c.-12-2730_-12-2729del	NP_001243412.1:n.-12-2730_-12-2729del
NM_001256484.2:c.-56-54_-56-53del	NP_001243413.1:n.-56-54_-56-53del
NM_001979.6:c.102-52_102-51del MANE Select	NP_001970.2:n.102-52_102-51del