Canonical Allele Identifier: CA1541874141

Gene: OXCT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41862655C= , CM000667.2:g.41862655C=	GRCh38
NC_000005.9:g.41862757C= , CM000667.1:g.41862757C=	GRCh37
NC_000005.8:g.41898514C=	NCBI36
NG_011823.1:g.13035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196371.10:c.174G= MANE Select	ENSP00000196371.5:p.Thr58=
ENST00000196371.9:c.174G=	ENSP00000196371.5:p.Thr58=
NM_000436.3:c.174G=	NP_000427.1:p.Thr58=
XR_427658.2:n.350G=
NM_001364299.1:c.174G=	NP_001351228.1:p.Thr58=
NM_001364300.1:c.195G=	NP_001351229.1:p.Thr65=
NM_001364301.1:c.174G=	NP_001351230.1:p.Thr58=
NM_001364302.1:c.174G=	NP_001351231.1:p.Thr58=
NR_157114.1:n.241G=
XR_001742081.2:n.351G=
NM_000436.4:c.174G= MANE Select	NP_000427.1:p.Thr58=
NM_001364299.2:c.174G=	NP_001351228.1:p.Thr58=
NM_001364300.2:c.195G=	NP_001351229.1:p.Thr65=
NM_001364301.2:c.174G=	NP_001351230.1:p.Thr58=
NM_001364302.2:c.174G=	NP_001351231.1:p.Thr58=
NR_157114.2:n.241G=