Canonical Allele Identifier: CA2397978618

Gene: SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23828766A= , CM000684.2:g.23828766A=	GRCh38
NC_000022.10:g.24170953A= , CM000684.1:g.24170953A=	GRCh37
NC_000022.9:g.22500953A=	NCBI36
NG_009303.1:g.46804A= , LRG_520:g.46804A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263121.12:c.848+3351A=	ENSP00000263121.8:n.848+3351A=
ENST00000344921.11:c.1013+3351A=	ENSP00000340883.6:n.1013+3351A=
ENST00000407422.8:c.959+3351A=	ENSP00000383984.3:n.959+3351A=
ENST00000477836.2:n.2137+3351A=
ENST00000644036.2:c.986+3351A= MANE Select	ENSP00000494049.2:n.986+3351A=
ENST00000644462.1:c.1704+3351A=	ENSP00000494283.1:n.1704+3351A=
ENST00000645799.1:n.2308+3351A=
ENST00000646723.1:n.3332+3351A=
ENST00000647057.1:c.*480+3351A=	ENSP00000494757.1:n.*480+3351A=
ENST00000263121.11:c.986+3351A=	ENSP00000263121.7:n.986+3351A=
ENST00000344921.10:c.1013+3351A=	ENSP00000340883.6:n.1013+3351A=
ENST00000407082.3:c.848+3351A=	ENSP00000385226.3:n.848+3351A=
ENST00000407422.7:c.959+3351A=	ENSP00000383984.3:n.959+3351A=
NM_001007468.1:c.959+3351A=	NP_001007469.1:n.959+3351A=
NM_003073.3:c.986+3351A= , LRG_520t1:c.986+3351A=	NP_003064.2:n.986+3351A=
XM_011530345.1:c.1040+3351A=	XP_011528647.1:n.1040+3351A=
XM_011530346.1:c.1013+3351A=	XP_011528648.1:n.1013+3351A=
NM_001007468.2:c.959+3351A=	NP_001007469.1:n.959+3351A=
NM_001317946.1:c.1013+3351A=	NP_001304875.1:n.1013+3351A=
NM_001362877.1:c.1040+3351A=	NP_001349806.1:n.1040+3351A=
NM_003073.4:c.986+3351A=	NP_003064.2:n.986+3351A=
NM_001007468.3:c.959+3351A=	NP_001007469.1:n.959+3351A=
NM_001317946.2:c.1013+3351A=	NP_001304875.1:n.1013+3351A=
NM_001362877.2:c.1040+3351A=	NP_001349806.1:n.1040+3351A=
NM_003073.5:c.986+3351A= MANE Select	NP_003064.2:n.986+3351A=