Canonical Allele Identifier: CA810733999

Gene: OXCT1

Linked Data

• dbSNP Id: rs1463414329
• MyVariant Identifiers: chr5:g.41862727A>G (hg19) ; chr5:g.41862625A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41862625A>G , CM000667.2:g.41862625A>G	GRCh38
NC_000005.9:g.41862727A>G , CM000667.1:g.41862727A>G	GRCh37
NC_000005.8:g.41898484A>G	NCBI36
NG_011823.1:g.13065T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196371.10:c.187+17T>C MANE Select	ENSP00000196371.5:n.187+17T>C
ENST00000196371.9:c.187+17T>C	ENSP00000196371.5:n.187+17T>C
NM_000436.3:c.187+17T>C	NP_000427.1:n.187+17T>C
XR_427658.2:n.363+17T>C
NM_001364299.1:c.187+17T>C	NP_001351228.1:n.187+17T>C
NM_001364300.1:c.208+17T>C	NP_001351229.1:n.208+17T>C
NM_001364301.1:c.187+17T>C	NP_001351230.1:n.187+17T>C
NM_001364302.1:c.187+17T>C	NP_001351231.1:n.187+17T>C
NR_157114.1:n.254+17T>C
XR_001742081.2:n.364+17T>C
NM_000436.4:c.187+17T>C MANE Select	NP_000427.1:n.187+17T>C
NM_001364299.2:c.187+17T>C	NP_001351228.1:n.187+17T>C
NM_001364300.2:c.208+17T>C	NP_001351229.1:n.208+17T>C
NM_001364301.2:c.187+17T>C	NP_001351230.1:n.187+17T>C
NM_001364302.2:c.187+17T>C	NP_001351231.1:n.187+17T>C
NR_157114.2:n.254+17T>C