Canonical Allele Identifier: CA1772845162

Gene: EPHX2

Linked Data

• dbSNP Id: rs1813740230

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27500883_27500888del , CM000670.2:g.27500883_27500888del	GRCh38
NC_000008.10:g.27358400_27358405del , CM000670.1:g.27358400_27358405del	GRCh37
NC_000008.9:g.27414317_27414322del	NCBI36
NG_012064.1:g.14756_14761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.102-43_102-38del MANE Select	ENSP00000430269.1:n.102-43_102-38del
ENST00000380476.7:c.-20-81_-20-76del	ENSP00000369843.3:n.-20-81_-20-76del
ENST00000517536.5:c.102-43_102-38del	ENSP00000428875.1:n.102-43_102-38del
ENST00000518328.5:c.102-43_102-38del	ENSP00000430779.1:n.102-43_102-38del
ENST00000518379.5:c.102-43_102-38del	ENSP00000427956.1:n.102-43_102-38del
ENST00000520623.5:n.186-43_186-38del
ENST00000520666.1:n.116-45_116-40del
ENST00000521400.5:c.102-43_102-38del	ENSP00000430269.1:n.102-43_102-38del
ENST00000521684.1:c.101-43_101-38del
ENST00000521780.5:c.-12-2721_-12-2716del	ENSP00000430302.1:n.-12-2721_-12-2716del
ENST00000523827.1:n.325-43_325-38del
NM_001256482.1:c.-20-81_-20-76del	NP_001243411.1:n.-20-81_-20-76del
NM_001256483.1:c.-12-2721_-12-2716del	NP_001243412.1:n.-12-2721_-12-2716del
NM_001256484.1:c.-56-45_-56-40del	NP_001243413.1:n.-56-45_-56-40del
NM_001979.5:c.102-43_102-38del	NP_001970.2:n.102-43_102-38del
XM_017013199.1:c.102-43_102-38del	XP_016868688.1:n.102-43_102-38del
XM_017013200.1:c.102-43_102-38del	XP_016868689.1:n.102-43_102-38del
XR_001745491.1:n.160-43_160-38del
NM_001256482.2:c.-20-81_-20-76del	NP_001243411.1:n.-20-81_-20-76del
NM_001256483.2:c.-12-2721_-12-2716del	NP_001243412.1:n.-12-2721_-12-2716del
NM_001256484.2:c.-56-45_-56-40del	NP_001243413.1:n.-56-45_-56-40del
NM_001979.6:c.102-43_102-38del MANE Select	NP_001970.2:n.102-43_102-38del