Canonical Allele Identifier: CA624957912

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1325373927
• gnomAD v2: 17-15932705-ATTT-A
• gnomAD v3: 17-16029391-ATTT-A
• gnomAD v4: 17-16029391-ATTT-A
• MyVariant Identifiers: chr17:g.15932706_15932708del (hg19) ; chr17:g.16029392_16029394del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029395_16029397del , CM000679.2:g.16029395_16029397del	GRCh38
NC_000017.10:g.15932709_15932711del , CM000679.1:g.15932709_15932711del	GRCh37
NC_000017.9:g.15873434_15873436del	NCBI36
NG_029806.1:g.35016_35018del
NG_047111.1:g.192353_192355del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2902_*2904del (NCOR1)	ENSP00000389839.2:n.*2902_*2904del
ENST00000704743.1:n.9173_9175del (NCOR1)
ENST00000704744.1:c.*2902_*2904del (NCOR1)	ENSP00000516021.1:n.*2902_*2904del
ENST00000704745.1:c.*2902_*2904del (NCOR1)	ENSP00000516022.1:n.*2902_*2904del
ENST00000261647.10:c.*1873_*1875del (TTC19) MANE Select	ENSP00000261647.5:n.*1873_*1875del
ENST00000268712.8:c.*2902_*2904del (NCOR1) MANE Select	ENSP00000268712.2:n.*2902_*2904del
ENST00000268712.7:c.*2902_*2904del (NCOR1)	ENSP00000268712.2:n.*2902_*2904del
ENST00000470649.1:c.247+2693_247+2695del (TTC19)	ENSP00000465627.1:n.247+2693_247+2695del
NM_001271420.1:c.*1873_*1875del (TTC19)	NP_001258349.1:n.*1873_*1875del
NM_017775.3:c.*1873_*1875del (TTC19)	NP_060245.3:n.*1873_*1875del
XM_017024801.2:c.994+2693_994+2695del (TTC19)	XP_016880290.2:n.994+2693_994+2695del
XM_017024802.2:c.994+2693_994+2695del (TTC19)	XP_016880291.2:n.994+2693_994+2695del
NM_006311.4:c.*2902_*2904del (NCOR1) MANE Select	NP_006302.2:n.*2902_*2904del
NM_017775.4:c.*1873_*1875del (TTC19) MANE Select	NP_060245.3:n.*1873_*1875del
NM_001271420.2:c.*1873_*1875del (TTC19)	NP_001258349.1:n.*1873_*1875del