Canonical Allele Identifier: CA624957902

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1407533884
• gnomAD v2: 17-15932626-C-T
• gnomAD v3: 17-16029312-C-T
• gnomAD v4: 17-16029312-C-T
• MyVariant Identifiers: chr17:g.15932626C>T (hg19) ; chr17:g.16029312C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029312C>T , CM000679.2:g.16029312C>T	GRCh38
NC_000017.10:g.15932626C>T , CM000679.1:g.15932626C>T	GRCh37
NC_000017.9:g.15873351C>T	NCBI36
NG_029806.1:g.34933C>T
NG_047111.1:g.192435G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2984G>A (NCOR1)	ENSP00000389839.2:n.*2984G>A
ENST00000704743.1:n.9255G>A (NCOR1)
ENST00000704744.1:c.*2984G>A (NCOR1)	ENSP00000516021.1:n.*2984G>A
ENST00000704745.1:c.*2984G>A (NCOR1)	ENSP00000516022.1:n.*2984G>A
ENST00000261647.10:c.*1790C>T (TTC19) MANE Select	ENSP00000261647.5:n.*1790C>T
ENST00000268712.8:c.*2984G>A (NCOR1) MANE Select	ENSP00000268712.2:n.*2984G>A
ENST00000268712.7:c.*2984G>A (NCOR1)	ENSP00000268712.2:n.*2984G>A
ENST00000470649.1:c.247+2610C>T (TTC19)	ENSP00000465627.1:n.247+2610C>T
NM_001271420.1:c.*1790C>T (TTC19)	NP_001258349.1:n.*1790C>T
NM_017775.3:c.*1790C>T (TTC19)	NP_060245.3:n.*1790C>T
XM_017024801.2:c.994+2610C>T (TTC19)	XP_016880290.2:n.994+2610C>T
XM_017024802.2:c.994+2610C>T (TTC19)	XP_016880291.2:n.994+2610C>T
NM_006311.4:c.*2984G>A (NCOR1) MANE Select	NP_006302.2:n.*2984G>A
NM_017775.4:c.*1790C>T (TTC19) MANE Select	NP_060245.3:n.*1790C>T
NM_001271420.2:c.*1790C>T (TTC19)	NP_001258349.1:n.*1790C>T