Canonical Allele Identifier: CA359627885

Gene: OXCT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41861399C>T , CM000667.2:g.41861399C>T	GRCh38
NC_000005.9:g.41861501C>T , CM000667.1:g.41861501C>T	GRCh37
NC_000005.8:g.41897258C>T	NCBI36
NG_011823.1:g.14291G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000436.4:c.193G>A MANE Select	NP_000427.1:p.Gly65Arg
ENST00000196371.10:c.193G>A MANE Select	ENSP00000196371.5:p.Gly65Arg
NM_000436.3:c.193G>A	NP_000427.1:p.Gly65Arg
NM_001364299.1:c.193G>A	NP_001351228.1:p.Gly65Arg
NM_001364299.2:c.193G>A	NP_001351228.1:p.Gly65Arg
NM_001364300.1:c.214G>A	NP_001351229.1:p.Gly72Arg
NM_001364300.2:c.214G>A	NP_001351229.1:p.Gly72Arg
NM_001364301.1:c.193G>A	NP_001351230.1:p.Gly65Arg
NM_001364301.2:c.193G>A	NP_001351230.1:p.Gly65Arg
NM_001364302.1:c.193G>A	NP_001351231.1:p.Gly65Arg
NM_001364302.2:c.193G>A	NP_001351231.1:p.Gly65Arg
NR_157114.1:n.260G>A
NR_157114.2:n.260G>A
ENST00000196371.9:c.193G>A	ENSP00000196371.5:p.Gly65Arg
XR_001742081.2:n.370G>A
XR_427658.2:n.369G>A