Canonical Allele Identifier: CA624957918

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs1265023127
• gnomAD v2: 17-15932790-CATT-C
• gnomAD v3: 17-16029476-CATT-C
• gnomAD v4: 17-16029476-CATT-C
• MyVariant Identifiers: chr17:g.15932791_15932793del (hg19) ; chr17:g.16029477_16029479del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029479_16029481del , CM000679.2:g.16029479_16029481del	GRCh38
NC_000017.10:g.15932793_15932795del , CM000679.1:g.15932793_15932795del	GRCh37
NC_000017.9:g.15873518_15873520del	NCBI36
NG_029806.1:g.35100_35102del
NG_047111.1:g.192268_192270del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.*2817_*2819del (NCOR1)	ENSP00000389839.2:n.*2817_*2819del
ENST00000704743.1:n.9088_9090del (NCOR1)
ENST00000704744.1:c.*2817_*2819del (NCOR1)	ENSP00000516021.1:n.*2817_*2819del
ENST00000704745.1:c.*2817_*2819del (NCOR1)	ENSP00000516022.1:n.*2817_*2819del
ENST00000268712.8:c.*2817_*2819del (NCOR1) MANE Select	ENSP00000268712.2:n.*2817_*2819del
ENST00000268712.7:c.*2817_*2819del (NCOR1)	ENSP00000268712.2:n.*2817_*2819del
ENST00000470649.1:c.247+2777_247+2779del (TTC19)	ENSP00000465627.1:n.247+2777_247+2779del
XM_017024801.2:c.994+2777_994+2779del (TTC19)	XP_016880290.2:n.994+2777_994+2779del
XM_017024802.2:c.994+2777_994+2779del (TTC19)	XP_016880291.2:n.994+2777_994+2779del
NM_006311.4:c.*2817_*2819del (NCOR1) MANE Select	NP_006302.2:n.*2817_*2819del