Canonical Allele Identifier: CA726464840

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1164262969
• MyVariant Identifiers: chr17:g.15932636_15932638del (hg19) ; chr17:g.16029322_16029324del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029326_16029328del , CM000679.2:g.16029326_16029328del	GRCh38
NC_000017.10:g.15932640_15932642del , CM000679.1:g.15932640_15932642del	GRCh37
NC_000017.9:g.15873365_15873367del	NCBI36
NG_029806.1:g.34947_34949del
NG_047111.1:g.192423_192425del

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2972_*2974del (NCOR1)	ENSP00000389839.2:n.*2972_*2974del
ENST00000704743.1:n.9243_9245del (NCOR1)
ENST00000704744.1:c.*2972_*2974del (NCOR1)	ENSP00000516021.1:n.*2972_*2974del
ENST00000704745.1:c.*2972_*2974del (NCOR1)	ENSP00000516022.1:n.*2972_*2974del
ENST00000261647.10:c.*1804_*1806del (TTC19) MANE Select	ENSP00000261647.5:n.*1804_*1806del
ENST00000268712.8:c.*2972_*2974del (NCOR1) MANE Select	ENSP00000268712.2:n.*2972_*2974del
ENST00000268712.7:c.*2972_*2974del (NCOR1)	ENSP00000268712.2:n.*2972_*2974del
ENST00000470649.1:c.247+2624_247+2626del (TTC19)	ENSP00000465627.1:n.247+2624_247+2626del
NM_001271420.1:c.*1804_*1806del (TTC19)	NP_001258349.1:n.*1804_*1806del
NM_017775.3:c.*1804_*1806del (TTC19)	NP_060245.3:n.*1804_*1806del
XM_017024801.2:c.994+2624_994+2626del (TTC19)	XP_016880290.2:n.994+2624_994+2626del
XM_017024802.2:c.994+2624_994+2626del (TTC19)	XP_016880291.2:n.994+2624_994+2626del
NM_006311.4:c.*2972_*2974del (NCOR1) MANE Select	NP_006302.2:n.*2972_*2974del
NM_017775.4:c.*1804_*1806del (TTC19) MANE Select	NP_060245.3:n.*1804_*1806del
NM_001271420.2:c.*1804_*1806del (TTC19)	NP_001258349.1:n.*1804_*1806del