Canonical Allele Identifier: CA180263

Gene: OXCT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41862717G>A , CM000667.2:g.41862717G>A	GRCh38
NC_000005.9:g.41862819G>A , CM000667.1:g.41862819G>A	GRCh37
NC_000005.8:g.41898576G>A	NCBI36
NG_011823.1:g.12973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196371.10:c.112C>T MANE Select	ENSP00000196371.5:p.Arg38Cys
ENST00000196371.9:c.112C>T	ENSP00000196371.5:p.Arg38Cys
NM_000436.3:c.112C>T	NP_000427.1:p.Arg38Cys
XR_427658.2:n.288C>T
NM_001364299.1:c.112C>T	NP_001351228.1:p.Arg38Cys
NM_001364300.1:c.133C>T	NP_001351229.1:p.Arg45Cys
NM_001364301.1:c.112C>T	NP_001351230.1:p.Arg38Cys
NM_001364302.1:c.112C>T	NP_001351231.1:p.Arg38Cys
NR_157114.1:n.179C>T
XR_001742081.2:n.289C>T
NM_000436.4:c.112C>T MANE Select	NP_000427.1:p.Arg38Cys
NM_001364299.2:c.112C>T	NP_001351228.1:p.Arg38Cys
NM_001364300.2:c.133C>T	NP_001351229.1:p.Arg45Cys
NM_001364301.2:c.112C>T	NP_001351230.1:p.Arg38Cys
NM_001364302.2:c.112C>T	NP_001351231.1:p.Arg38Cys
NR_157114.2:n.179C>T