Canonical Allele Identifier: CA1541874108

Gene: OXCT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41862619A= , CM000667.2:g.41862619A=	GRCh38
NC_000005.9:g.41862721A= , CM000667.1:g.41862721A=	GRCh37
NC_000005.8:g.41898478A=	NCBI36
NG_011823.1:g.13071T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000196371.10:c.187+23T= MANE Select	ENSP00000196371.5:n.187+23T=
ENST00000196371.9:c.187+23T=	ENSP00000196371.5:n.187+23T=
NM_000436.3:c.187+23T=	NP_000427.1:n.187+23T=
XR_427658.2:n.363+23T=
NM_001364299.1:c.187+23T=	NP_001351228.1:n.187+23T=
NM_001364300.1:c.208+23T=	NP_001351229.1:n.208+23T=
NM_001364301.1:c.187+23T=	NP_001351230.1:n.187+23T=
NM_001364302.1:c.187+23T=	NP_001351231.1:n.187+23T=
NR_157114.1:n.254+23T=
XR_001742081.2:n.364+23T=
NM_000436.4:c.187+23T= MANE Select	NP_000427.1:n.187+23T=
NM_001364299.2:c.187+23T=	NP_001351228.1:n.187+23T=
NM_001364300.2:c.208+23T=	NP_001351229.1:n.208+23T=
NM_001364301.2:c.187+23T=	NP_001351230.1:n.187+23T=
NM_001364302.2:c.187+23T=	NP_001351231.1:n.187+23T=
NR_157114.2:n.254+23T=