Canonical Allele Identifier: CA981833457

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1251471814
• gnomAD v3: 17-16029518-C-G
• gnomAD v4: 17-16029518-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029518C>G , CM000679.2:g.16029518C>G	GRCh38
NC_000017.10:g.15932832C>G , CM000679.1:g.15932832C>G	GRCh37
NC_000017.9:g.15873557C>G	NCBI36
NG_029806.1:g.35139C>G
NG_047111.1:g.192229G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2778G>C (NCOR1)	ENSP00000389839.2:n.*2778G>C
ENST00000704743.1:n.9049G>C (NCOR1)
ENST00000704744.1:c.*2778G>C (NCOR1)	ENSP00000516021.1:n.*2778G>C
ENST00000704745.1:c.*2778G>C (NCOR1)	ENSP00000516022.1:n.*2778G>C
ENST00000268712.8:c.*2778G>C (NCOR1) MANE Select	ENSP00000268712.2:n.*2778G>C
ENST00000268712.7:c.*2778G>C (NCOR1)	ENSP00000268712.2:n.*2778G>C
ENST00000470649.1:c.247+2816C>G (TTC19)	ENSP00000465627.1:n.247+2816C>G
XM_017024801.2:c.994+2816C>G (TTC19)	XP_016880290.2:n.994+2816C>G
XM_017024802.2:c.994+2816C>G (TTC19)	XP_016880291.2:n.994+2816C>G
NM_006311.4:c.*2778G>C (NCOR1) MANE Select	NP_006302.2:n.*2778G>C