Canonical Allele Identifier: CA1541862176

Gene: OXCT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41853358C= , CM000667.2:g.41853358C=	GRCh38
NC_000005.9:g.41853460C= , CM000667.1:g.41853460C=	GRCh37
NC_000005.8:g.41889217C=	NCBI36
NG_011823.1:g.22332G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000196371.10:c.414+61G= MANE Select	ENSP00000196371.5:n.414+61G=
ENST00000196371.9:c.414+61G=	ENSP00000196371.5:n.414+61G=
NM_000436.3:c.414+61G=	NP_000427.1:n.414+61G=
XR_427658.2:n.590+61G=
NM_001364299.1:c.414+61G=	NP_001351228.1:n.414+61G=
NM_001364300.1:c.435+61G=	NP_001351229.1:n.435+61G=
NM_001364301.1:c.414+61G=	NP_001351230.1:n.414+61G=
NM_001364302.1:c.414+61G=	NP_001351231.1:n.414+61G=
NR_157114.1:n.481+61G=
XR_001742081.2:n.591+61G=
NM_000436.4:c.414+61G= MANE Select	NP_000427.1:n.414+61G=
NM_001364299.2:c.414+61G=	NP_001351228.1:n.414+61G=
NM_001364300.2:c.435+61G=	NP_001351229.1:n.435+61G=
NM_001364301.2:c.414+61G=	NP_001351230.1:n.414+61G=
NM_001364302.2:c.414+61G=	NP_001351231.1:n.414+61G=
NR_157114.2:n.481+61G=