Canonical Allele Identifier: CA2636264904
Gene: NCOR1 HGNC NCBI
TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-16029417-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16029417G>T , CM000679.2:g.16029417G>T GRCh38
NC_000017.10:g.15932731G>T , CM000679.1:g.15932731G>T GRCh37
NC_000017.9:g.15873456G>T NCBI36
NG_029806.1:g.35038G>T
NG_047111.1:g.192330C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000436068.2:c.*2879C>A (NCOR1) ENSP00000389839.2:n.*2879C>A
ENST00000704743.1:n.9150C>A (NCOR1)
ENST00000704744.1:c.*2879C>A (NCOR1) ENSP00000516021.1:n.*2879C>A
ENST00000704745.1:c.*2879C>A (NCOR1) ENSP00000516022.1:n.*2879C>A
ENST00000268712.8:c.*2879C>A (NCOR1) MANE Select ENSP00000268712.2:n.*2879C>A
ENST00000268712.7:c.*2879C>A (NCOR1) ENSP00000268712.2:n.*2879C>A
ENST00000470649.1:c.247+2715G>T (TTC19) ENSP00000465627.1:n.247+2715G>T
XM_017024801.2:c.994+2715G>T (TTC19) XP_016880290.2:n.994+2715G>T
XM_017024802.2:c.994+2715G>T (TTC19) XP_016880291.2:n.994+2715G>T
NM_006311.4:c.*2879C>A (NCOR1) MANE Select NP_006302.2:n.*2879C>A
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