Canonical Allele Identifier: CA2249873228

Gene: NCOR1 TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029330T= , CM000679.2:g.16029330T=	GRCh38
NC_000017.10:g.15932644T= , CM000679.1:g.15932644T=	GRCh37
NC_000017.9:g.15873369T=	NCBI36
NG_029806.1:g.34951T=
NG_047111.1:g.192417A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2966A= (NCOR1)	ENSP00000389839.2:n.*2966A=
ENST00000704743.1:n.9237A= (NCOR1)
ENST00000704744.1:c.*2966A= (NCOR1)	ENSP00000516021.1:n.*2966A=
ENST00000704745.1:c.*2966A= (NCOR1)	ENSP00000516022.1:n.*2966A=
ENST00000261647.10:c.*1808T= (TTC19) MANE Select	ENSP00000261647.5:n.*1808T=
ENST00000268712.8:c.*2966A= (NCOR1) MANE Select	ENSP00000268712.2:n.*2966A=
ENST00000268712.7:c.*2966A= (NCOR1)	ENSP00000268712.2:n.*2966A=
ENST00000470649.1:c.247+2628T= (TTC19)	ENSP00000465627.1:n.247+2628T=
NM_001271420.1:c.*1808T= (TTC19)	NP_001258349.1:n.*1808T=
NM_017775.3:c.*1808T= (TTC19)	NP_060245.3:n.*1808T=
XM_017024801.2:c.994+2628T= (TTC19)	XP_016880290.2:n.994+2628T=
XM_017024802.2:c.994+2628T= (TTC19)	XP_016880291.2:n.994+2628T=
NM_006311.4:c.*2966A= (NCOR1) MANE Select	NP_006302.2:n.*2966A=
NM_017775.4:c.*1808T= (TTC19) MANE Select	NP_060245.3:n.*1808T=
NM_001271420.2:c.*1808T= (TTC19)	NP_001258349.1:n.*1808T=