Canonical Allele Identifier: CA2397961263

Gene: SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23793404_23793405delinsCT , CM000684.2:g.23793404_23793405delinsCT	GRCh38
NC_000022.10:g.24135591_24135592delinsCT , CM000684.1:g.24135591_24135592delinsCT	GRCh37
NC_000022.9:g.22465591_22465592delinsCT	NCBI36
NG_009303.1:g.11442_11443delinsCT , LRG_520:g.11442_11443delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.233-155_233-154delinsCT	ENSP00000263121.8:n.233-155_233-154delinsCT
ENST00000344921.11:c.206-155_206-154delinsCT	ENSP00000340883.6:n.206-155_206-154delinsCT
ENST00000407082.4:c.206-155_206-154delinsCT	ENSP00000385226.4:n.206-155_206-154delinsCT
ENST00000407422.8:c.206-155_206-154delinsCT	ENSP00000383984.3:n.206-155_206-154delinsCT
ENST00000417137.6:c.233-155_233-154delinsCT	ENSP00000388489.2:n.233-155_233-154delinsCT
ENST00000491967.2:n.396-155_396-154delinsCT
ENST00000643421.1:n.201-155_201-154delinsCT
ENST00000644036.2:c.233-155_233-154delinsCT MANE Select	ENSP00000494049.2:n.233-155_233-154delinsCT
ENST00000644462.1:c.68-155_68-154delinsCT	ENSP00000494283.1:n.68-155_68-154delinsCT
ENST00000644619.1:c.233-155_233-154delinsCT	ENSP00000494695.1:n.233-155_233-154delinsCT
ENST00000646421.1:n.1934_1935delinsCT
ENST00000646723.1:n.221-155_221-154delinsCT
ENST00000646911.1:n.145-155_145-154delinsCT
ENST00000647057.1:c.93+6142_93+6143delinsCT	ENSP00000494757.1:n.93+6142_93+6143delinsCT
ENST00000263121.11:c.233-155_233-154delinsCT	ENSP00000263121.7:n.233-155_233-154delinsCT
ENST00000344921.10:c.206-155_206-154delinsCT	ENSP00000340883.6:n.206-155_206-154delinsCT
ENST00000407082.3:c.233-155_233-154delinsCT	ENSP00000385226.3:n.233-155_233-154delinsCT
ENST00000407422.7:c.206-155_206-154delinsCT	ENSP00000383984.3:n.206-155_206-154delinsCT
ENST00000417137.5:c.233-155_233-154delinsCT	ENSP00000388489.1:n.233-155_233-154delinsCT
ENST00000634926.1:c.85-155_85-154delinsCT
ENST00000635578.1:c.58-155_58-154delinsCT
NM_001007468.1:c.206-155_206-154delinsCT	NP_001007469.1:n.206-155_206-154delinsCT
NM_003073.3:c.233-155_233-154delinsCT , LRG_520t1:c.233-155_233-154delinsCT	NP_003064.2:n.233-155_233-154delinsCT
XM_011530345.1:c.233-155_233-154delinsCT	XP_011528647.1:n.233-155_233-154delinsCT
XM_011530346.1:c.206-155_206-154delinsCT	XP_011528648.1:n.206-155_206-154delinsCT
NM_001007468.2:c.206-155_206-154delinsCT	NP_001007469.1:n.206-155_206-154delinsCT
NM_001317946.1:c.206-155_206-154delinsCT	NP_001304875.1:n.206-155_206-154delinsCT
NM_001362877.1:c.233-155_233-154delinsCT	NP_001349806.1:n.233-155_233-154delinsCT
NM_003073.4:c.233-155_233-154delinsCT	NP_003064.2:n.233-155_233-154delinsCT
NM_001007468.3:c.206-155_206-154delinsCT	NP_001007469.1:n.206-155_206-154delinsCT
NM_001317946.2:c.206-155_206-154delinsCT	NP_001304875.1:n.206-155_206-154delinsCT
NM_001362877.2:c.233-155_233-154delinsCT	NP_001349806.1:n.233-155_233-154delinsCT
NM_003073.5:c.233-155_233-154delinsCT MANE Select	NP_003064.2:n.233-155_233-154delinsCT