Canonical Allele Identifier: CA2063244441

Gene: CUX2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111322507C= , CM000674.2:g.111322507C=	GRCh38
NC_000012.11:g.111760311C= , CM000674.1:g.111760311C=	GRCh37
NC_000012.10:g.110244694C=	NCBI36
NG_023039.1:g.293484C=
NG_023039.2:g.293484C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015267.4:c.2853C= MANE Select	NP_056082.2:p.Pro951=
ENST00000261726.11:c.2853C= MANE Select	ENSP00000261726.6:p.Pro951=
NM_001370598.1:c.2667C=	NP_001357527.1:p.Pro889=
NM_015267.3:c.2853C=	NP_056082.2:p.Pro951=
ENST00000261726.10:c.2853C=	ENSP00000261726.6:p.Pro951=
XM_011538061.1:c.3021C=	XP_011536363.1:p.Pro1007=
XM_011538061.3:c.3021C=	XP_011536363.1:p.Pro1007=
XM_011538062.1:c.2910C=	XP_011536364.1:p.Pro970=
XM_011538063.1:c.2886C=	XP_011536365.1:p.Pro962=
XM_011538063.3:c.2886C=	XP_011536365.1:p.Pro962=
XM_011538064.1:c.2829C=	XP_011536366.1:p.Pro943=
XM_011538065.1:c.2667C=	XP_011536367.1:p.Pro889=
XM_011538066.1:c.2667C=	XP_011536368.1:p.Pro889=
XM_011538067.1:c.2667C=	XP_011536369.1:p.Pro889=
XM_011538068.1:c.2667C=	XP_011536370.1:p.Pro889=
XM_011538069.1:c.2667C=	XP_011536371.1:p.Pro889=
XM_011538069.2:c.2667C=	XP_011536371.1:p.Pro889=
XM_011538070.1:c.2667C=	XP_011536372.1:p.Pro889=
XM_011538070.2:c.2667C=	XP_011536372.1:p.Pro889=
XM_011538071.1:c.2667C=	XP_011536373.1:p.Pro889=
XM_011538072.1:c.2667C=	XP_011536374.1:p.Pro889=
XM_017019080.1:c.2667C=	XP_016874569.1:p.Pro889=
XM_017019081.1:c.2667C=	XP_016874570.1:p.Pro889=