Canonical Allele Identifier: CA031340
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 242800
dbSNP Id: rs75134564
gnomAD v2: 5-41862758-G-A
gnomAD v3: 5-41862656-G-A
gnomAD v4: 5-41862656-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41862656G>A , CM000667.2:g.41862656G>A GRCh38
NC_000005.9:g.41862758G>A , CM000667.1:g.41862758G>A GRCh37
NC_000005.8:g.41898515G>A NCBI36
NG_011823.1:g.13034C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000196371.10:c.173C>T MANE Select ENSP00000196371.5:p.Thr58Met
ENST00000196371.9:c.173C>T ENSP00000196371.5:p.Thr58Met
NM_000436.3:c.173C>T NP_000427.1:p.Thr58Met
XR_427658.2:n.349C>T
NM_001364299.1:c.173C>T NP_001351228.1:p.Thr58Met
NM_001364300.1:c.194C>T NP_001351229.1:p.Thr65Met
NM_001364301.1:c.173C>T NP_001351230.1:p.Thr58Met
NM_001364302.1:c.173C>T NP_001351231.1:p.Thr58Met
NR_157114.1:n.240C>T
XR_001742081.2:n.350C>T
NM_000436.4:c.173C>T MANE Select NP_000427.1:p.Thr58Met
NM_001364299.2:c.173C>T NP_001351228.1:p.Thr58Met
NM_001364300.2:c.194C>T NP_001351229.1:p.Thr65Met
NM_001364301.2:c.173C>T NP_001351230.1:p.Thr58Met
NM_001364302.2:c.173C>T NP_001351231.1:p.Thr58Met
NR_157114.2:n.240C>T