Canonical Allele Identifier: CA2249873429

Gene: NCOR1 TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029476_16029479delinsCATT , CM000679.2:g.16029476_16029479delinsCATT	GRCh38
NC_000017.10:g.15932790_15932793delinsCATT , CM000679.1:g.15932790_15932793delinsCATT	GRCh37
NC_000017.9:g.15873515_15873518delinsCATT	NCBI36
NG_029806.1:g.35097_35100delinsCATT
NG_047111.1:g.192268_192271delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2817_*2820delinsAATG (NCOR1)	ENSP00000389839.2:n.*2817_*2820delinsAATG
ENST00000704743.1:n.9088_9091delinsAATG (NCOR1)
ENST00000704744.1:c.*2817_*2820delinsAATG (NCOR1)	ENSP00000516021.1:n.*2817_*2820delinsAATG
ENST00000704745.1:c.*2817_*2820delinsAATG (NCOR1)	ENSP00000516022.1:n.*2817_*2820delinsAATG
ENST00000268712.8:c.*2817_*2820delinsAATG (NCOR1) MANE Select	ENSP00000268712.2:n.*2817_*2820delinsAATG
ENST00000268712.7:c.*2817_*2820delinsAATG (NCOR1)	ENSP00000268712.2:n.*2817_*2820delinsAATG
ENST00000470649.1:c.247+2774_247+2777delinsCATT (TTC19)	ENSP00000465627.1:n.247+2774_247+2777delinsCATT
XM_017024801.2:c.994+2774_994+2777delinsCATT (TTC19)	XP_016880290.2:n.994+2774_994+2777delinsCATT
XM_017024802.2:c.994+2774_994+2777delinsCATT (TTC19)	XP_016880291.2:n.994+2774_994+2777delinsCATT
NM_006311.4:c.*2817_*2820delinsAATG (NCOR1) MANE Select	NP_006302.2:n.*2817_*2820delinsAATG