Canonical Allele Identifier: CA4244130

Gene: OGDH

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44700236A>G , CM000669.2:g.44700236A>G	GRCh38
NC_000007.13:g.44739835A>G , CM000669.1:g.44739835A>G	GRCh37
NC_000007.12:g.44706360A>G	NCBI36
NG_023260.1:g.98715A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447398.6:c.2559A>G	ENSP00000388183.1:p.Leu853=
ENST00000222673.6:c.2526A>G MANE Select	ENSP00000222673.5:p.Leu842=
ENST00000222673.5:c.2526A>G	ENSP00000222673.5:p.Leu842=
ENST00000439616.6:c.2076A>G	ENSP00000398576.2:p.Leu692=
ENST00000444676.5:c.2571A>G	ENSP00000414662.1:p.Leu857=
ENST00000447398.5:c.2559A>G	ENSP00000388183.1:p.Leu853=
ENST00000449767.5:c.2514A>G	ENSP00000392878.1:p.Leu838=
ENST00000631326.2:c.2523A>G	ENSP00000486854.1:p.Leu841=
NM_001165036.1:c.2514A>G	NP_001158508.1:p.Leu838=
NM_002541.3:c.2526A>G	NP_002532.2:p.Leu842=
XM_005249759.3:c.2571A>G	XP_005249816.1:p.Leu857=
XM_005249761.2:c.2559A>G	XP_005249818.1:p.Leu853=
XM_011515408.1:c.2571A>G	XP_011513710.1:p.Leu857=
NM_001363523.1:c.2559A>G	NP_001350452.1:p.Leu853=
XM_005249759.5:c.2571A>G	XP_005249816.1:p.Leu857=
XM_011515408.2:c.2571A>G	XP_011513710.1:p.Leu857=
XM_024446783.1:c.1911A>G	XP_024302551.1:p.Leu637=
NM_002541.4:c.2526A>G MANE Select	NP_002532.2:p.Leu842=
NM_001165036.2:c.2514A>G	NP_001158508.1:p.Leu838=
NM_001363523.2:c.2559A>G	NP_001350452.1:p.Leu853=