Canonical Allele Identifier: CA1541862158

Gene: OXCT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41853344C= , CM000667.2:g.41853344C=	GRCh38
NC_000005.9:g.41853446C= , CM000667.1:g.41853446C=	GRCh37
NC_000005.8:g.41889203C=	NCBI36
NG_011823.1:g.22346G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000196371.10:c.414+75G= MANE Select	ENSP00000196371.5:n.414+75G=
ENST00000196371.9:c.414+75G=	ENSP00000196371.5:n.414+75G=
NM_000436.3:c.414+75G=	NP_000427.1:n.414+75G=
XR_427658.2:n.590+75G=
NM_001364299.1:c.414+75G=	NP_001351228.1:n.414+75G=
NM_001364300.1:c.435+75G=	NP_001351229.1:n.435+75G=
NM_001364301.1:c.414+75G=	NP_001351230.1:n.414+75G=
NM_001364302.1:c.414+75G=	NP_001351231.1:n.414+75G=
NR_157114.1:n.481+75G=
XR_001742081.2:n.591+75G=
NM_000436.4:c.414+75G= MANE Select	NP_000427.1:n.414+75G=
NM_001364299.2:c.414+75G=	NP_001351228.1:n.414+75G=
NM_001364300.2:c.435+75G=	NP_001351229.1:n.435+75G=
NM_001364301.2:c.414+75G=	NP_001351230.1:n.414+75G=
NM_001364302.2:c.414+75G=	NP_001351231.1:n.414+75G=
NR_157114.2:n.481+75G=