Canonical Allele Identifier: CA2249873408

Gene: NCOR1 TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029459T= , CM000679.2:g.16029459T=	GRCh38
NC_000017.10:g.15932773T= , CM000679.1:g.15932773T=	GRCh37
NC_000017.9:g.15873498T=	NCBI36
NG_029806.1:g.35080T=
NG_047111.1:g.192288A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2837A= (NCOR1)	ENSP00000389839.2:n.*2837A=
ENST00000704743.1:n.9108A= (NCOR1)
ENST00000704744.1:c.*2837A= (NCOR1)	ENSP00000516021.1:n.*2837A=
ENST00000704745.1:c.*2837A= (NCOR1)	ENSP00000516022.1:n.*2837A=
ENST00000268712.8:c.*2837A= (NCOR1) MANE Select	ENSP00000268712.2:n.*2837A=
ENST00000268712.7:c.*2837A= (NCOR1)	ENSP00000268712.2:n.*2837A=
ENST00000470649.1:c.247+2757T= (TTC19)	ENSP00000465627.1:n.247+2757T=
XM_017024801.2:c.994+2757T= (TTC19)	XP_016880290.2:n.994+2757T=
XM_017024802.2:c.994+2757T= (TTC19)	XP_016880291.2:n.994+2757T=
NM_006311.4:c.*2837A= (NCOR1) MANE Select	NP_006302.2:n.*2837A=