Canonical Allele Identifier: CA443805252

Gene: OXCT1

Linked Data

• MyVariant Identifiers: chr5:g.41862757C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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