Canonical Allele Identifier: CA4243690

Gene: OGDH

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44675162C>T , CM000669.2:g.44675162C>T	GRCh38
NC_000007.13:g.44714761C>T , CM000669.1:g.44714761C>T	GRCh37
NC_000007.12:g.44681286C>T	NCBI36
NG_023260.1:g.73641C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447398.6:c.969-16C>T	ENSP00000388183.1:n.969-16C>T
ENST00000222673.6:c.936-16C>T MANE Select	ENSP00000222673.5:n.936-16C>T
ENST00000222673.5:c.936-16C>T	ENSP00000222673.5:n.936-16C>T
ENST00000439616.6:c.486-16C>T	ENSP00000398576.2:n.486-16C>T
ENST00000443864.6:c.936-16C>T	ENSP00000388084.2:n.936-16C>T
ENST00000444676.5:c.981-16C>T	ENSP00000414662.1:n.981-16C>T
ENST00000447398.5:c.969-16C>T	ENSP00000388183.1:n.969-16C>T
ENST00000449767.5:c.924-16C>T	ENSP00000392878.1:n.924-16C>T
ENST00000459672.5:n.534-16C>T
ENST00000631326.2:c.936-16C>T	ENSP00000486854.1:n.936-16C>T
NM_001003941.2:c.936-16C>T	NP_001003941.1:n.936-16C>T
NM_001165036.1:c.924-16C>T	NP_001158508.1:n.924-16C>T
NM_002541.3:c.936-16C>T	NP_002532.2:n.936-16C>T
XM_005249759.3:c.981-16C>T	XP_005249816.1:n.981-16C>T
XM_005249761.2:c.969-16C>T	XP_005249818.1:n.969-16C>T
XM_011515408.1:c.981-16C>T	XP_011513710.1:n.981-16C>T
NM_001363523.1:c.969-16C>T	NP_001350452.1:n.969-16C>T
XM_005249759.5:c.981-16C>T	XP_005249816.1:n.981-16C>T
XM_011515408.2:c.981-16C>T	XP_011513710.1:n.981-16C>T
XM_024446783.1:c.321-16C>T	XP_024302551.1:n.321-16C>T
NM_002541.4:c.936-16C>T MANE Select	NP_002532.2:n.936-16C>T
NM_001003941.3:c.936-16C>T	NP_001003941.1:n.936-16C>T
NM_001165036.2:c.924-16C>T	NP_001158508.1:n.924-16C>T
NM_001363523.2:c.969-16C>T	NP_001350452.1:n.969-16C>T