Canonical Allele Identifier: CA031415
Gene: OXCT1 HGNC NCBI

Linked Data

dbSNP Id: rs267606930
MyVariant Identifiers: chr5:g.41853537A>T (hg19) chr5:g.41853435A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41853435A>T , CM000667.2:g.41853435A>T GRCh38
NC_000005.9:g.41853537A>T , CM000667.1:g.41853537A>T GRCh37
NC_000005.8:g.41889294A>T NCBI36
NG_011823.1:g.22255T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000196371.10:c.398T>A MANE Select ENSP00000196371.5:p.Val133Glu
ENST00000196371.9:c.398T>A ENSP00000196371.5:p.Val133Glu
NM_000436.3:c.398T>A NP_000427.1:p.Val133Glu
XR_427658.2:n.574T>A
NM_001364299.1:c.398T>A NP_001351228.1:p.Val133Glu
NM_001364300.1:c.419T>A NP_001351229.1:p.Val140Glu
NM_001364301.1:c.398T>A NP_001351230.1:p.Val133Glu
NM_001364302.1:c.398T>A NP_001351231.1:p.Val133Glu
NR_157114.1:n.465T>A
XR_001742081.2:n.575T>A
NM_000436.4:c.398T>A MANE Select NP_000427.1:p.Val133Glu
NM_001364299.2:c.398T>A NP_001351228.1:p.Val133Glu
NM_001364300.2:c.419T>A NP_001351229.1:p.Val140Glu
NM_001364301.2:c.398T>A NP_001351230.1:p.Val133Glu
NM_001364302.2:c.398T>A NP_001351231.1:p.Val133Glu
NR_157114.2:n.465T>A
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