Canonical Allele Identifier: CA2397961282

Gene: SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23793450_23793451delinsCT , CM000684.2:g.23793450_23793451delinsCT	GRCh38
NC_000022.10:g.24135637_24135638delinsCT , CM000684.1:g.24135637_24135638delinsCT	GRCh37
NC_000022.9:g.22465637_22465638delinsCT	NCBI36
NG_009303.1:g.11488_11489delinsCT , LRG_520:g.11488_11489delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.233-109_233-108delinsCT	ENSP00000263121.8:n.233-109_233-108delinsCT
ENST00000344921.11:c.206-109_206-108delinsCT	ENSP00000340883.6:n.206-109_206-108delinsCT
ENST00000407082.4:c.206-109_206-108delinsCT	ENSP00000385226.4:n.206-109_206-108delinsCT
ENST00000407422.8:c.206-109_206-108delinsCT	ENSP00000383984.3:n.206-109_206-108delinsCT
ENST00000417137.6:c.233-109_233-108delinsCT	ENSP00000388489.2:n.233-109_233-108delinsCT
ENST00000491967.2:n.396-109_396-108delinsCT
ENST00000643421.1:n.201-109_201-108delinsCT
ENST00000644036.2:c.233-109_233-108delinsCT MANE Select	ENSP00000494049.2:n.233-109_233-108delinsCT
ENST00000644462.1:c.68-109_68-108delinsCT	ENSP00000494283.1:n.68-109_68-108delinsCT
ENST00000644619.1:c.233-109_233-108delinsCT	ENSP00000494695.1:n.233-109_233-108delinsCT
ENST00000646421.1:n.1980_1981delinsCT
ENST00000646723.1:n.221-109_221-108delinsCT
ENST00000646911.1:n.145-109_145-108delinsCT
ENST00000647057.1:c.93+6188_93+6189delinsCT	ENSP00000494757.1:n.93+6188_93+6189delinsCT
ENST00000263121.11:c.233-109_233-108delinsCT	ENSP00000263121.7:n.233-109_233-108delinsCT
ENST00000344921.10:c.206-109_206-108delinsCT	ENSP00000340883.6:n.206-109_206-108delinsCT
ENST00000407082.3:c.233-109_233-108delinsCT	ENSP00000385226.3:n.233-109_233-108delinsCT
ENST00000407422.7:c.206-109_206-108delinsCT	ENSP00000383984.3:n.206-109_206-108delinsCT
ENST00000417137.5:c.233-109_233-108delinsCT	ENSP00000388489.1:n.233-109_233-108delinsCT
ENST00000634926.1:c.85-109_85-108delinsCT
ENST00000635578.1:c.58-109_58-108delinsCT
NM_001007468.1:c.206-109_206-108delinsCT	NP_001007469.1:n.206-109_206-108delinsCT
NM_003073.3:c.233-109_233-108delinsCT , LRG_520t1:c.233-109_233-108delinsCT	NP_003064.2:n.233-109_233-108delinsCT
XM_011530345.1:c.233-109_233-108delinsCT	XP_011528647.1:n.233-109_233-108delinsCT
XM_011530346.1:c.206-109_206-108delinsCT	XP_011528648.1:n.206-109_206-108delinsCT
NM_001007468.2:c.206-109_206-108delinsCT	NP_001007469.1:n.206-109_206-108delinsCT
NM_001317946.1:c.206-109_206-108delinsCT	NP_001304875.1:n.206-109_206-108delinsCT
NM_001362877.1:c.233-109_233-108delinsCT	NP_001349806.1:n.233-109_233-108delinsCT
NM_003073.4:c.233-109_233-108delinsCT	NP_003064.2:n.233-109_233-108delinsCT
NM_001007468.3:c.206-109_206-108delinsCT	NP_001007469.1:n.206-109_206-108delinsCT
NM_001317946.2:c.206-109_206-108delinsCT	NP_001304875.1:n.206-109_206-108delinsCT
NM_001362877.2:c.233-109_233-108delinsCT	NP_001349806.1:n.233-109_233-108delinsCT
NM_003073.5:c.233-109_233-108delinsCT MANE Select	NP_003064.2:n.233-109_233-108delinsCT