Canonical Allele Identifier: CA4244293

Gene: OGDH

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44707995C>T , CM000669.2:g.44707995C>T	GRCh38
NC_000007.13:g.44747594C>T , CM000669.1:g.44747594C>T	GRCh37
NC_000007.12:g.44714119C>T	NCBI36
NG_023260.1:g.106474C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447398.6:c.3101C>T	ENSP00000388183.1:p.Ser1034Leu
ENST00000222673.6:c.3068C>T MANE Select	ENSP00000222673.5:p.Ser1023Leu
ENST00000222673.5:c.3068C>T	ENSP00000222673.5:p.Ser1023Leu
ENST00000439616.6:c.2618C>T	ENSP00000398576.2:p.Ser873Leu
ENST00000444676.5:c.3113C>T	ENSP00000414662.1:p.Ser1038Leu
ENST00000447398.5:c.3101C>T	ENSP00000388183.1:p.Ser1034Leu
ENST00000449767.5:c.3056C>T	ENSP00000392878.1:p.Ser1019Leu
ENST00000631326.2:c.*58C>T	ENSP00000486854.1:n.*58C>T
NM_001165036.1:c.3056C>T	NP_001158508.1:p.Ser1019Leu
NM_002541.3:c.3068C>T	NP_002532.2:p.Ser1023Leu
XM_005249759.3:c.3113C>T	XP_005249816.1:p.Ser1038Leu
XM_005249761.2:c.3101C>T	XP_005249818.1:p.Ser1034Leu
XM_011515408.1:c.3113C>T	XP_011513710.1:p.Ser1038Leu
NM_001363523.1:c.3101C>T	NP_001350452.1:p.Ser1034Leu
XM_005249759.5:c.3113C>T	XP_005249816.1:p.Ser1038Leu
XM_011515408.2:c.3113C>T	XP_011513710.1:p.Ser1038Leu
XM_024446783.1:c.2453C>T	XP_024302551.1:p.Ser818Leu
NM_002541.4:c.3068C>T MANE Select	NP_002532.2:p.Ser1023Leu
NM_001165036.2:c.3056C>T	NP_001158508.1:p.Ser1019Leu
NM_001363523.2:c.3101C>T	NP_001350452.1:p.Ser1034Leu