Canonical Allele Identifier: CA2249873106

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1597477553

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029254A>G , CM000679.2:g.16029254A>G	GRCh38
NC_000017.10:g.15932568A>G , CM000679.1:g.15932568A>G	GRCh37
NC_000017.9:g.15873293A>G	NCBI36
NG_029806.1:g.34875A>G
NG_047111.1:g.192493T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*3042T>C (NCOR1)	ENSP00000389839.2:n.*3042T>C
ENST00000704743.1:n.9313T>C (NCOR1)
ENST00000704744.1:c.*3042T>C (NCOR1)	ENSP00000516021.1:n.*3042T>C
ENST00000704745.1:c.*3042T>C (NCOR1)	ENSP00000516022.1:n.*3042T>C
ENST00000261647.10:c.*1732A>G (TTC19) MANE Select	ENSP00000261647.5:n.*1732A>G
ENST00000268712.8:c.*3042T>C (NCOR1) MANE Select	ENSP00000268712.2:n.*3042T>C
ENST00000268712.7:c.*3042T>C (NCOR1)	ENSP00000268712.2:n.*3042T>C
ENST00000470649.1:c.247+2552A>G (TTC19)	ENSP00000465627.1:n.247+2552A>G
NM_001271420.1:c.*1732A>G (TTC19)	NP_001258349.1:n.*1732A>G
NM_017775.3:c.*1732A>G (TTC19)	NP_060245.3:n.*1732A>G
XM_017024801.2:c.994+2552A>G (TTC19)	XP_016880290.2:n.994+2552A>G
XM_017024802.2:c.994+2552A>G (TTC19)	XP_016880291.2:n.994+2552A>G
NM_006311.4:c.*3042T>C (NCOR1) MANE Select	NP_006302.2:n.*3042T>C
NM_017775.4:c.*1732A>G (TTC19) MANE Select	NP_060245.3:n.*1732A>G
NM_001271420.2:c.*1732A>G (TTC19)	NP_001258349.1:n.*1732A>G