Canonical Allele Identifier: CA410932442

Gene: SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23791772G>C , CM000684.2:g.23791772G>C	GRCh38
NC_000022.10:g.24133959G>C , CM000684.1:g.24133959G>C	GRCh37
NC_000022.9:g.22463959G>C	NCBI36
NG_009303.1:g.9810G>C , LRG_520:g.9810G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003073.5:c.110G>C MANE Select	NP_003064.2:p.Arg37Pro
ENST00000644036.2:c.110G>C MANE Select	ENSP00000494049.2:p.Arg37Pro
NM_001007468.1:c.110G>C	NP_001007469.1:p.Arg37Pro
NM_001007468.2:c.110G>C	NP_001007469.1:p.Arg37Pro
NM_001007468.3:c.110G>C	NP_001007469.1:p.Arg37Pro
NM_001317946.1:c.110G>C	NP_001304875.1:p.Arg37Pro
NM_001317946.2:c.110G>C	NP_001304875.1:p.Arg37Pro
NM_001362877.1:c.110G>C	NP_001349806.1:p.Arg37Pro
NM_001362877.2:c.110G>C	NP_001349806.1:p.Arg37Pro
NM_003073.3:c.110G>C , LRG_520t1:c.110G>C	NP_003064.2:p.Arg37Pro
NM_003073.4:c.110G>C	NP_003064.2:p.Arg37Pro
ENST00000263121.11:c.110G>C	ENSP00000263121.7:p.Arg37Pro
ENST00000263121.12:c.110G>C	ENSP00000263121.8:p.Arg37Pro
ENST00000344921.10:c.110G>C	ENSP00000340883.6:p.Arg37Pro
ENST00000344921.11:c.110G>C	ENSP00000340883.6:p.Arg37Pro
ENST00000407082.3:c.110G>C	ENSP00000385226.3:p.Arg37Pro
ENST00000407082.4:c.110G>C	ENSP00000385226.4:p.Arg37Pro
ENST00000407422.7:c.110G>C	ENSP00000383984.3:p.Arg37Pro
ENST00000407422.8:c.110G>C	ENSP00000383984.3:p.Arg37Pro
ENST00000417137.5:c.110G>C	ENSP00000388489.1:p.Arg37Pro
ENST00000417137.6:c.110G>C	ENSP00000388489.2:p.Arg37Pro
ENST00000491967.2:n.300G>C
ENST00000643421.1:n.78G>C
ENST00000644619.1:c.110G>C	ENSP00000494695.1:p.Arg37Pro
ENST00000646421.1:n.302G>C
ENST00000646723.1:n.98G>C
ENST00000646911.1:n.22G>C
ENST00000647057.1:c.93+4510G>C	ENSP00000494757.1:n.93+4510G>C
XM_011530345.1:c.110G>C	XP_011528647.1:p.Arg37Pro
XM_011530346.1:c.110G>C	XP_011528648.1:p.Arg37Pro