Canonical Allele Identifier: CA2636264845
Gene: NCOR1 HGNC NCBI
TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-16029330-TG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16029331del , CM000679.2:g.16029331del GRCh38
NC_000017.10:g.15932645del , CM000679.1:g.15932645del GRCh37
NC_000017.9:g.15873370del NCBI36
NG_029806.1:g.34952del
NG_047111.1:g.192416del

Transcript Alleles

HGVS Amino-acid change
ENST00000436068.2:c.*2965del (NCOR1) ENSP00000389839.2:n.*2965del
ENST00000704743.1:n.9236del (NCOR1)
ENST00000704744.1:c.*2965del (NCOR1) ENSP00000516021.1:n.*2965del
ENST00000704745.1:c.*2965del (NCOR1) ENSP00000516022.1:n.*2965del
ENST00000261647.10:c.*1809del (TTC19) MANE Select ENSP00000261647.5:n.*1809del
ENST00000268712.8:c.*2965del (NCOR1) MANE Select ENSP00000268712.2:n.*2965del
ENST00000268712.7:c.*2965del (NCOR1) ENSP00000268712.2:n.*2965del
ENST00000470649.1:c.247+2629del (TTC19) ENSP00000465627.1:n.247+2629del
NM_001271420.1:c.*1809del (TTC19) NP_001258349.1:n.*1809del
NM_017775.3:c.*1809del (TTC19) NP_060245.3:n.*1809del
XM_017024801.2:c.994+2629del (TTC19) XP_016880290.2:n.994+2629del
XM_017024802.2:c.994+2629del (TTC19) XP_016880291.2:n.994+2629del
NM_006311.4:c.*2965del (NCOR1) MANE Select NP_006302.2:n.*2965del
NM_017775.4:c.*1809del (TTC19) MANE Select NP_060245.3:n.*1809del
NM_001271420.2:c.*1809del (TTC19) NP_001258349.1:n.*1809del
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