Canonical Allele Identifier: CA981833433

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1971759392
• gnomAD v3: 17-16029427-G-A
• gnomAD v4: 17-16029427-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029427G>A , CM000679.2:g.16029427G>A	GRCh38
NC_000017.10:g.15932741G>A , CM000679.1:g.15932741G>A	GRCh37
NC_000017.9:g.15873466G>A	NCBI36
NG_029806.1:g.35048G>A
NG_047111.1:g.192320C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2869C>T (NCOR1)	ENSP00000389839.2:n.*2869C>T
ENST00000704743.1:n.9140C>T (NCOR1)
ENST00000704744.1:c.*2869C>T (NCOR1)	ENSP00000516021.1:n.*2869C>T
ENST00000704745.1:c.*2869C>T (NCOR1)	ENSP00000516022.1:n.*2869C>T
ENST00000268712.8:c.*2869C>T (NCOR1) MANE Select	ENSP00000268712.2:n.*2869C>T
ENST00000268712.7:c.*2869C>T (NCOR1)	ENSP00000268712.2:n.*2869C>T
ENST00000470649.1:c.247+2725G>A (TTC19)	ENSP00000465627.1:n.247+2725G>A
XM_017024801.2:c.994+2725G>A (TTC19)	XP_016880290.2:n.994+2725G>A
XM_017024802.2:c.994+2725G>A (TTC19)	XP_016880291.2:n.994+2725G>A
NM_006311.4:c.*2869C>T (NCOR1) MANE Select	NP_006302.2:n.*2869C>T