Canonical Allele Identifier: CA454865810

Gene: OGDH

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44697707C>T , CM000669.2:g.44697707C>T	GRCh38
NC_000007.13:g.44737306C>T , CM000669.1:g.44737306C>T	GRCh37
NC_000007.12:g.44703831C>T	NCBI36
NG_023260.1:g.96186C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447398.6:c.2316C>T	ENSP00000388183.1:p.Phe772=
ENST00000222673.6:c.2283C>T MANE Select	ENSP00000222673.5:p.Phe761=
ENST00000222673.5:c.2283C>T	ENSP00000222673.5:p.Phe761=
ENST00000439616.6:c.1833C>T	ENSP00000398576.2:p.Phe611=
ENST00000444676.5:c.2328C>T	ENSP00000414662.1:p.Phe776=
ENST00000447398.5:c.2316C>T	ENSP00000388183.1:p.Phe772=
ENST00000449767.5:c.2271C>T	ENSP00000392878.1:p.Phe757=
ENST00000631326.2:c.2280C>T	ENSP00000486854.1:p.Phe760=
NM_001165036.1:c.2271C>T	NP_001158508.1:p.Phe757=
NM_002541.3:c.2283C>T	NP_002532.2:p.Phe761=
XM_005249759.3:c.2328C>T	XP_005249816.1:p.Phe776=
XM_005249761.2:c.2316C>T	XP_005249818.1:p.Phe772=
XM_011515408.1:c.2328C>T	XP_011513710.1:p.Phe776=
NM_001363523.1:c.2316C>T	NP_001350452.1:p.Phe772=
XM_005249759.5:c.2328C>T	XP_005249816.1:p.Phe776=
XM_011515408.2:c.2328C>T	XP_011513710.1:p.Phe776=
XM_024446783.1:c.1668C>T	XP_024302551.1:p.Phe556=
NM_002541.4:c.2283C>T MANE Select	NP_002532.2:p.Phe761=
NM_001165036.2:c.2271C>T	NP_001158508.1:p.Phe757=
NM_001363523.2:c.2316C>T	NP_001350452.1:p.Phe772=