Canonical Allele Identifier: CA2636264960
Gene: NCOR1 HGNC NCBI
TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-16029476-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16029476C>A , CM000679.2:g.16029476C>A GRCh38
NC_000017.10:g.15932790C>A , CM000679.1:g.15932790C>A GRCh37
NC_000017.9:g.15873515C>A NCBI36
NG_029806.1:g.35097C>A
NG_047111.1:g.192271G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000436068.2:c.*2820G>T (NCOR1) ENSP00000389839.2:n.*2820G>T
ENST00000704743.1:n.9091G>T (NCOR1)
ENST00000704744.1:c.*2820G>T (NCOR1) ENSP00000516021.1:n.*2820G>T
ENST00000704745.1:c.*2820G>T (NCOR1) ENSP00000516022.1:n.*2820G>T
ENST00000268712.8:c.*2820G>T (NCOR1) MANE Select ENSP00000268712.2:n.*2820G>T
ENST00000268712.7:c.*2820G>T (NCOR1) ENSP00000268712.2:n.*2820G>T
ENST00000470649.1:c.247+2774C>A (TTC19) ENSP00000465627.1:n.247+2774C>A
XM_017024801.2:c.994+2774C>A (TTC19) XP_016880290.2:n.994+2774C>A
XM_017024802.2:c.994+2774C>A (TTC19) XP_016880291.2:n.994+2774C>A
NM_006311.4:c.*2820G>T (NCOR1) MANE Select NP_006302.2:n.*2820G>T
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