Canonical Allele Identifier: CA2636265102

Gene: NCOR1 TTC19

Linked Data

• gnomAD v4: 17-16029541-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029541G>A , CM000679.2:g.16029541G>A	GRCh38
NC_000017.10:g.15932855G>A , CM000679.1:g.15932855G>A	GRCh37
NC_000017.9:g.15873580G>A	NCBI36
NG_029806.1:g.35162G>A
NG_047111.1:g.192206C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2755C>T (NCOR1)	ENSP00000389839.2:n.*2755C>T
ENST00000704743.1:n.9026C>T (NCOR1)
ENST00000704744.1:c.*2755C>T (NCOR1)	ENSP00000516021.1:n.*2755C>T
ENST00000704745.1:c.*2755C>T (NCOR1)	ENSP00000516022.1:n.*2755C>T
ENST00000268712.8:c.*2755C>T (NCOR1) MANE Select	ENSP00000268712.2:n.*2755C>T
ENST00000268712.7:c.*2755C>T (NCOR1)	ENSP00000268712.2:n.*2755C>T
ENST00000470649.1:c.247+2839G>A (TTC19)	ENSP00000465627.1:n.247+2839G>A
XM_017024801.2:c.994+2839G>A (TTC19)	XP_016880290.2:n.994+2839G>A
XM_017024802.2:c.994+2839G>A (TTC19)	XP_016880291.2:n.994+2839G>A
NM_006311.4:c.*2755C>T (NCOR1) MANE Select	NP_006302.2:n.*2755C>T