Canonical Allele Identifier: CA726464887

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1170764052
• MyVariant Identifiers: chr17:g.15932862G>C (hg19) ; chr17:g.16029548G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029548G>C , CM000679.2:g.16029548G>C	GRCh38
NC_000017.10:g.15932862G>C , CM000679.1:g.15932862G>C	GRCh37
NC_000017.9:g.15873587G>C	NCBI36
NG_029806.1:g.35169G>C
NG_047111.1:g.192199C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2748C>G (NCOR1)	ENSP00000389839.2:n.*2748C>G
ENST00000704743.1:n.9019C>G (NCOR1)
ENST00000704744.1:c.*2748C>G (NCOR1)	ENSP00000516021.1:n.*2748C>G
ENST00000704745.1:c.*2748C>G (NCOR1)	ENSP00000516022.1:n.*2748C>G
ENST00000268712.8:c.*2748C>G (NCOR1) MANE Select	ENSP00000268712.2:n.*2748C>G
ENST00000268712.7:c.*2748C>G (NCOR1)	ENSP00000268712.2:n.*2748C>G
ENST00000470649.1:c.247+2846G>C (TTC19)	ENSP00000465627.1:n.247+2846G>C
XM_017024801.2:c.994+2846G>C (TTC19)	XP_016880290.2:n.994+2846G>C
XM_017024802.2:c.994+2846G>C (TTC19)	XP_016880291.2:n.994+2846G>C
NM_006311.4:c.*2748C>G (NCOR1) MANE Select	NP_006302.2:n.*2748C>G