Canonical Allele Identifier: CA288166841

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs757498040
• MyVariant Identifiers: chr17:g.15932768C>G (hg19) ; chr17:g.16029454C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029454C>G , CM000679.2:g.16029454C>G	GRCh38
NC_000017.10:g.15932768C>G , CM000679.1:g.15932768C>G	GRCh37
NC_000017.9:g.15873493C>G	NCBI36
NG_029806.1:g.35075C>G
NG_047111.1:g.192293G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2842G>C (NCOR1)	ENSP00000389839.2:n.*2842G>C
ENST00000704743.1:n.9113G>C (NCOR1)
ENST00000704744.1:c.*2842G>C (NCOR1)	ENSP00000516021.1:n.*2842G>C
ENST00000704745.1:c.*2842G>C (NCOR1)	ENSP00000516022.1:n.*2842G>C
ENST00000268712.8:c.*2842G>C (NCOR1) MANE Select	ENSP00000268712.2:n.*2842G>C
ENST00000268712.7:c.*2842G>C (NCOR1)	ENSP00000268712.2:n.*2842G>C
ENST00000470649.1:c.247+2752C>G (TTC19)	ENSP00000465627.1:n.247+2752C>G
XM_017024801.2:c.994+2752C>G (TTC19)	XP_016880290.2:n.994+2752C>G
XM_017024802.2:c.994+2752C>G (TTC19)	XP_016880291.2:n.994+2752C>G
NM_006311.4:c.*2842G>C (NCOR1) MANE Select	NP_006302.2:n.*2842G>C