Canonical Allele Identifier: CA2397958142

Gene: SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23787086_23787112delinsCCCTCGGCCCAGCACGCCCCGGCCCCG , CM000684.2:g.23787086_23787112delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	GRCh38
NC_000022.10:g.24129273_24129299delinsCCCTCGGCCCAGCACGCCCCGGCCCCG , CM000684.1:g.24129273_24129299delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	GRCh37
NC_000022.9:g.22459273_22459299delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NCBI36
NG_009303.1:g.5124_5150delinsCCCTCGGCCCAGCACGCCCCGGCCCCG , LRG_520:g.5124_5150delinsCCCTCGGCCCAGCACGCCCCGGCCCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000263121.12:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000263121.8:n.-84_-58delinsCCCTCGGC...
ENST00000344921.11:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000340883.6:n.-84_-58delinsCCCTCGGC...
ENST00000407082.4:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000385226.4:n.-84_-58delinsCCCTCGGC...
ENST00000407422.8:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000383984.3:n.-84_-58delinsCCCTCGGC...
ENST00000417137.6:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000388489.2:n.-84_-58delinsCCCTCGGC...
ENST00000491967.2:n.107_133delinsCCCTCGGCCCAGCACGCCCCGGCCCCG
ENST00000644036.2:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG MANE Select	ENSP00000494049.2:n.-84_-58delinsCCCTCGGC...
ENST00000644619.1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000494695.1:n.-84_-58delinsCCCTCGGC...
ENST00000646421.1:n.109_135delinsCCCTCGGCCCAGCACGCCCCGGCCCCG
ENST00000647057.1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000494757.1:n.-84_-58delinsCCCTCGGC...
ENST00000263121.11:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000263121.7:n.-84_-58delinsCCCTCGGC...
ENST00000344921.10:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000340883.6:n.-84_-58delinsCCCTCGGC...
ENST00000407082.3:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000385226.3:n.-84_-58delinsCCCTCGGC...
ENST00000407422.7:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000383984.3:n.-84_-58delinsCCCTCGGC...
ENST00000417137.5:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	ENSP00000388489.1:n.-84_-58delinsCCCTCGGC...
NM_001007468.1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_001007469.1:n.-84_-58delinsCCCTCGGCCCA...
NM_003073.3:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG , LRG_520t1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_003064.2:n.-84_-58delinsCCCTCGGCCCAGCA...
XM_011530345.1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	XP_011528647.1:n.-84_-58delinsCCCTCGGCCCA...
XM_011530346.1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	XP_011528648.1:n.-84_-58delinsCCCTCGGCCCA...
NM_001007468.2:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_001007469.1:n.-84_-58delinsCCCTCGGCCCA...
NM_001317946.1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_001304875.1:n.-84_-58delinsCCCTCGGCCCA...
NM_001362877.1:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_001349806.1:n.-84_-58delinsCCCTCGGCCCA...
NM_003073.4:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_003064.2:n.-84_-58delinsCCCTCGGCCCAGCA...
NM_001007468.3:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_001007469.1:n.-84_-58delinsCCCTCGGCCCA...
NM_001317946.2:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_001304875.1:n.-84_-58delinsCCCTCGGCCCA...
NM_001362877.2:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG	NP_001349806.1:n.-84_-58delinsCCCTCGGCCCA...
NM_003073.5:c.-84_-58delinsCCCTCGGCCCAGCACGCCCCGGCCCCG MANE Select	NP_003064.2:n.-84_-58delinsCCCTCGGCCCAGCA...