Canonical Allele Identifier: CA359627933

Gene: OXCT1

Linked Data

• MyVariant Identifiers: chr5:g.41862755A>C (hg19) ; chr5:g.41862653A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41862653A>C , CM000667.2:g.41862653A>C	GRCh38
NC_000005.9:g.41862755A>C , CM000667.1:g.41862755A>C	GRCh37
NC_000005.8:g.41898512A>C	NCBI36
NG_011823.1:g.13037T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196371.10:c.176T>G MANE Select	ENSP00000196371.5:p.Val59Gly
ENST00000196371.9:c.176T>G	ENSP00000196371.5:p.Val59Gly
NM_000436.3:c.176T>G	NP_000427.1:p.Val59Gly
XR_427658.2:n.352T>G
NM_001364299.1:c.176T>G	NP_001351228.1:p.Val59Gly
NM_001364300.1:c.197T>G	NP_001351229.1:p.Val66Gly
NM_001364301.1:c.176T>G	NP_001351230.1:p.Val59Gly
NM_001364302.1:c.176T>G	NP_001351231.1:p.Val59Gly
NR_157114.1:n.243T>G
XR_001742081.2:n.353T>G
NM_000436.4:c.176T>G MANE Select	NP_000427.1:p.Val59Gly
NM_001364299.2:c.176T>G	NP_001351228.1:p.Val59Gly
NM_001364300.2:c.197T>G	NP_001351229.1:p.Val66Gly
NM_001364301.2:c.176T>G	NP_001351230.1:p.Val59Gly
NM_001364302.2:c.176T>G	NP_001351231.1:p.Val59Gly
NR_157114.2:n.243T>G