Canonical Allele Identifier: CA2249873224

Gene: NCOR1 TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029327G= , CM000679.2:g.16029327G=	GRCh38
NC_000017.10:g.15932641G= , CM000679.1:g.15932641G=	GRCh37
NC_000017.9:g.15873366G=	NCBI36
NG_029806.1:g.34948G=
NG_047111.1:g.192420C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2969C= (NCOR1)	ENSP00000389839.2:n.*2969C=
ENST00000704743.1:n.9240C= (NCOR1)
ENST00000704744.1:c.*2969C= (NCOR1)	ENSP00000516021.1:n.*2969C=
ENST00000704745.1:c.*2969C= (NCOR1)	ENSP00000516022.1:n.*2969C=
ENST00000261647.10:c.*1805G= (TTC19) MANE Select	ENSP00000261647.5:n.*1805G=
ENST00000268712.8:c.*2969C= (NCOR1) MANE Select	ENSP00000268712.2:n.*2969C=
ENST00000268712.7:c.*2969C= (NCOR1)	ENSP00000268712.2:n.*2969C=
ENST00000470649.1:c.247+2625G= (TTC19)	ENSP00000465627.1:n.247+2625G=
NM_001271420.1:c.*1805G= (TTC19)	NP_001258349.1:n.*1805G=
NM_017775.3:c.*1805G= (TTC19)	NP_060245.3:n.*1805G=
XM_017024801.2:c.994+2625G= (TTC19)	XP_016880290.2:n.994+2625G=
XM_017024802.2:c.994+2625G= (TTC19)	XP_016880291.2:n.994+2625G=
NM_006311.4:c.*2969C= (NCOR1) MANE Select	NP_006302.2:n.*2969C=
NM_017775.4:c.*1805G= (TTC19) MANE Select	NP_060245.3:n.*1805G=
NM_001271420.2:c.*1805G= (TTC19)	NP_001258349.1:n.*1805G=