Canonical Allele Identifier: CA2397981113

Gene: SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23834188A= , CM000684.2:g.23834188A=	GRCh38
NC_000022.10:g.24176375A= , CM000684.1:g.24176375A=	GRCh37
NC_000022.9:g.22506375A=	NCBI36
NG_009303.1:g.52226A= , LRG_520:g.52226A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.*8A=	ENSP00000263121.8:n.*8A=
ENST00000344921.11:c.*8A=	ENSP00000340883.6:n.*8A=
ENST00000407422.8:c.*8A=	ENSP00000383984.3:n.*8A=
ENST00000644036.2:c.*8A= MANE Select	ENSP00000494049.2:n.*8A=
ENST00000644462.1:c.1884A=	ENSP00000494283.1:n.1884A=
ENST00000645799.1:n.2488A=
ENST00000646723.1:n.3512A=
ENST00000647057.1:c.*660A=	ENSP00000494757.1:n.*660A=
ENST00000263121.11:c.*8A=	ENSP00000263121.7:n.*8A=
ENST00000344921.10:c.*8A=	ENSP00000340883.6:n.*8A=
ENST00000407422.7:c.*8A=	ENSP00000383984.3:n.*8A=
NM_001007468.1:c.*8A=	NP_001007469.1:n.*8A=
NM_003073.3:c.*8A= , LRG_520t1:c.*8A=	NP_003064.2:n.*8A=
XM_011530345.1:c.*8A=	XP_011528647.1:n.*8A=
XM_011530346.1:c.*8A=	XP_011528648.1:n.*8A=
NM_001007468.2:c.*8A=	NP_001007469.1:n.*8A=
NM_001317946.1:c.*8A=	NP_001304875.1:n.*8A=
NM_001362877.1:c.*8A=	NP_001349806.1:n.*8A=
NM_003073.4:c.*8A=	NP_003064.2:n.*8A=
NM_001007468.3:c.*8A=	NP_001007469.1:n.*8A=
NM_001317946.2:c.*8A=	NP_001304875.1:n.*8A=
NM_001362877.2:c.*8A=	NP_001349806.1:n.*8A=
NM_003073.5:c.*8A= MANE Select	NP_003064.2:n.*8A=