Canonical Allele Identifier: CA288166836

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs966001171
• gnomAD v2: 17-15932747-A-C
• gnomAD v3: 17-16029433-A-C
• gnomAD v4: 17-16029433-A-C
• MyVariant Identifiers: chr17:g.15932747A>C (hg19) ; chr17:g.16029433A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029433A>C , CM000679.2:g.16029433A>C	GRCh38
NC_000017.10:g.15932747A>C , CM000679.1:g.15932747A>C	GRCh37
NC_000017.9:g.15873472A>C	NCBI36
NG_029806.1:g.35054A>C
NG_047111.1:g.192314T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2863T>G (NCOR1)	ENSP00000389839.2:n.*2863T>G
ENST00000704743.1:n.9134T>G (NCOR1)
ENST00000704744.1:c.*2863T>G (NCOR1)	ENSP00000516021.1:n.*2863T>G
ENST00000704745.1:c.*2863T>G (NCOR1)	ENSP00000516022.1:n.*2863T>G
ENST00000268712.8:c.*2863T>G (NCOR1) MANE Select	ENSP00000268712.2:n.*2863T>G
ENST00000268712.7:c.*2863T>G (NCOR1)	ENSP00000268712.2:n.*2863T>G
ENST00000470649.1:c.247+2731A>C (TTC19)	ENSP00000465627.1:n.247+2731A>C
XM_017024801.2:c.994+2731A>C (TTC19)	XP_016880290.2:n.994+2731A>C
XM_017024802.2:c.994+2731A>C (TTC19)	XP_016880291.2:n.994+2731A>C
NM_006311.4:c.*2863T>G (NCOR1) MANE Select	NP_006302.2:n.*2863T>G