Canonical Allele Identifier: CA2636265000
Gene: NCOR1 HGNC NCBI
TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-16029483-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16029483A>C , CM000679.2:g.16029483A>C GRCh38
NC_000017.10:g.15932797A>C , CM000679.1:g.15932797A>C GRCh37
NC_000017.9:g.15873522A>C NCBI36
NG_029806.1:g.35104A>C
NG_047111.1:g.192264T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000436068.2:c.*2813T>G (NCOR1) ENSP00000389839.2:n.*2813T>G
ENST00000704743.1:n.9084T>G (NCOR1)
ENST00000704744.1:c.*2813T>G (NCOR1) ENSP00000516021.1:n.*2813T>G
ENST00000704745.1:c.*2813T>G (NCOR1) ENSP00000516022.1:n.*2813T>G
ENST00000268712.8:c.*2813T>G (NCOR1) MANE Select ENSP00000268712.2:n.*2813T>G
ENST00000268712.7:c.*2813T>G (NCOR1) ENSP00000268712.2:n.*2813T>G
ENST00000470649.1:c.247+2781A>C (TTC19) ENSP00000465627.1:n.247+2781A>C
XM_017024801.2:c.994+2781A>C (TTC19) XP_016880290.2:n.994+2781A>C
XM_017024802.2:c.994+2781A>C (TTC19) XP_016880291.2:n.994+2781A>C
NM_006311.4:c.*2813T>G (NCOR1) MANE Select NP_006302.2:n.*2813T>G
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