Canonical Allele Identifier: CA2580077176

Gene: OGDH

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44675961C>T , CM000669.2:g.44675961C>T	GRCh38
NC_000007.13:g.44715560C>T , CM000669.1:g.44715560C>T	GRCh37
NC_000007.12:g.44682085C>T	NCBI36
NG_023260.1:g.74440C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447398.6:c.1060-9C>T	ENSP00000388183.1:n.1060-9C>T
ENST00000222673.6:c.1027-9C>T MANE Select	ENSP00000222673.5:n.1027-9C>T
ENST00000222673.5:c.1027-9C>T	ENSP00000222673.5:n.1027-9C>T
ENST00000439616.6:c.577-9C>T	ENSP00000398576.2:n.577-9C>T
ENST00000443864.6:c.1027-9C>T	ENSP00000388084.2:n.1027-9C>T
ENST00000444676.5:c.1072-9C>T	ENSP00000414662.1:n.1072-9C>T
ENST00000447398.5:c.1060-9C>T	ENSP00000388183.1:n.1060-9C>T
ENST00000449767.5:c.1015-9C>T	ENSP00000392878.1:n.1015-9C>T
ENST00000631326.2:c.1027-9C>T	ENSP00000486854.1:n.1027-9C>T
NM_001003941.2:c.1027-9C>T	NP_001003941.1:n.1027-9C>T
NM_001165036.1:c.1015-9C>T	NP_001158508.1:n.1015-9C>T
NM_002541.3:c.1027-9C>T	NP_002532.2:n.1027-9C>T
XM_005249759.3:c.1072-9C>T	XP_005249816.1:n.1072-9C>T
XM_005249761.2:c.1060-9C>T	XP_005249818.1:n.1060-9C>T
XM_011515408.1:c.1072-9C>T	XP_011513710.1:n.1072-9C>T
NM_001363523.1:c.1060-9C>T	NP_001350452.1:n.1060-9C>T
XM_005249759.5:c.1072-9C>T	XP_005249816.1:n.1072-9C>T
XM_011515408.2:c.1072-9C>T	XP_011513710.1:n.1072-9C>T
XM_024446783.1:c.412-9C>T	XP_024302551.1:n.412-9C>T
NM_002541.4:c.1027-9C>T MANE Select	NP_002532.2:n.1027-9C>T
NM_001003941.3:c.1027-9C>T	NP_001003941.1:n.1027-9C>T
NM_001165036.2:c.1015-9C>T	NP_001158508.1:n.1015-9C>T
NM_001363523.2:c.1060-9C>T	NP_001350452.1:n.1060-9C>T