Canonical Allele Identifier: CA2249873383

Gene: NCOR1 TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029450_16029454delinsATCAC , CM000679.2:g.16029450_16029454delinsATCAC	GRCh38
NC_000017.10:g.15932764_15932768delinsATCAC , CM000679.1:g.15932764_15932768delinsATCAC	GRCh37
NC_000017.9:g.15873489_15873493delinsATCAC	NCBI36
NG_029806.1:g.35071_35075delinsATCAC
NG_047111.1:g.192293_192297delinsGTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2842_*2846delinsGTGAT (NCOR1)	ENSP00000389839.2:n.*2842_*2846delinsGTGAT
ENST00000704743.1:n.9113_9117delinsGTGAT (NCOR1)
ENST00000704744.1:c.*2842_*2846delinsGTGAT (NCOR1)	ENSP00000516021.1:n.*2842_*2846delinsGTGAT
ENST00000704745.1:c.*2842_*2846delinsGTGAT (NCOR1)	ENSP00000516022.1:n.*2842_*2846delinsGTGAT
ENST00000268712.8:c.*2842_*2846delinsGTGAT (NCOR1) MANE Select	ENSP00000268712.2:n.*2842_*2846delinsGTGAT
ENST00000268712.7:c.*2842_*2846delinsGTGAT (NCOR1)	ENSP00000268712.2:n.*2842_*2846delinsGTGAT
ENST00000470649.1:c.247+2748_247+2752delinsATCAC (TTC19)	ENSP00000465627.1:n.247+2748_247+2752delinsATCAC
XM_017024801.2:c.994+2748_994+2752delinsATCAC (TTC19)	XP_016880290.2:n.994+2748_994+2752delinsATCAC
XM_017024802.2:c.994+2748_994+2752delinsATCAC (TTC19)	XP_016880291.2:n.994+2748_994+2752delinsATCAC
NM_006311.4:c.*2842_*2846delinsGTGAT (NCOR1) MANE Select	NP_006302.2:n.*2842_*2846delinsGTGAT