Canonical Allele Identifier: CA10824923

Gene: EPHX1 TMEM63A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225844317G>A , CM000663.2:g.225844317G>A	GRCh38
NC_000001.10:g.226032018G>A , CM000663.1:g.226032018G>A	GRCh37
NC_000001.9:g.224098641G>A	NCBI36
NG_009776.1:g.39222G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001136018.4:c.1041-181G>A (EPHX1) MANE Select	NP_001129490.1:n.1041-181G>A
ENST00000272167.10:c.1041-181G>A (EPHX1) MANE Select	ENSP00000272167.5:n.1041-181G>A
NM_000120.3:c.1041-181G>A (EPHX1)	NP_000111.1:n.1041-181G>A
NM_000120.4:c.1041-181G>A (EPHX1)	NP_000111.1:n.1041-181G>A
NM_001136018.3:c.1041-181G>A (EPHX1)	NP_001129490.1:n.1041-181G>A
NM_001291163.1:c.1041-181G>A (EPHX1)	NP_001278092.1:n.1041-181G>A
NM_001291163.2:c.1041-181G>A (EPHX1)	NP_001278092.1:n.1041-181G>A
NM_001378426.1:c.1041-181G>A (EPHX1)	NP_001365355.1:n.1041-181G>A
NM_001378427.1:c.1041-181G>A (EPHX1)	NP_001365356.1:n.1041-181G>A
NM_001378428.1:c.1014-181G>A (EPHX1)	NP_001365357.1:n.1014-181G>A
NM_001378429.1:c.993-181G>A (EPHX1)	NP_001365358.1:n.993-181G>A
NM_001378430.1:c.993-181G>A (EPHX1)	NP_001365359.1:n.993-181G>A
NM_001378431.1:c.813-181G>A (EPHX1)	NP_001365360.1:n.813-181G>A
NM_001378432.1:c.474-181G>A (EPHX1)	NP_001365361.1:n.474-181G>A
NR_165624.1:n.431-181G>A (EPHX1)
NR_165625.1:n.1016-181G>A (EPHX1)
NR_165626.1:n.1429-181G>A (EPHX1)
NR_165627.1:n.1161-181G>A (EPHX1)
ENST00000272167.9:c.1041-181G>A (EPHX1)	ENSP00000272167.5:n.1041-181G>A
ENST00000366837.5:c.1041-181G>A (EPHX1)	ENSP00000355802.4:n.1041-181G>A
ENST00000614058.4:c.1041-181G>A (EPHX1)	ENSP00000480004.1:n.1041-181G>A
XR_949163.1:n.2830+2521C>T (TMEM63A)
XR_949163.3:n.2809+2521C>T (TMEM63A)