Canonical Allele Identifier: CA410935446

Gene: SMARCB1

Linked Data

• MyVariant Identifiers: chr22:g.24145491C>G (hg19) ; chr22:g.23803304C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23803304C>G , CM000684.2:g.23803304C>G	GRCh38
NC_000022.10:g.24145491C>G , CM000684.1:g.24145491C>G	GRCh37
NC_000022.9:g.22475491C>G	NCBI36
NG_009303.1:g.21342C>G , LRG_520:g.21342C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263121.12:c.372C>G	ENSP00000263121.8:p.Asp124Glu
ENST00000344921.11:c.537C>G	ENSP00000340883.6:p.Asp179Glu
ENST00000407082.4:c.345C>G	ENSP00000385226.4:p.Asp115Glu
ENST00000407422.8:c.483C>G	ENSP00000383984.3:p.Asp161Glu
ENST00000417137.6:c.564C>G	ENSP00000388489.2:p.Asp188Glu
ENST00000642275.1:n.758C>G
ENST00000642727.1:c.676C>G	ENSP00000495144.1:n.676C>G
ENST00000643421.1:n.478C>G
ENST00000644036.2:c.510C>G MANE Select	ENSP00000494049.2:p.Asp170Glu
ENST00000644462.1:c.1228C>G	ENSP00000494283.1:n.1228C>G
ENST00000644467.1:n.1304C>G
ENST00000644619.1:c.*577C>G	ENSP00000494695.1:n.*577C>G
ENST00000646723.1:n.2711C>G
ENST00000646911.1:n.422C>G
ENST00000647057.1:c.*4C>G	ENSP00000494757.1:n.*4C>G
ENST00000263121.11:c.510C>G	ENSP00000263121.7:p.Asp170Glu
ENST00000344921.10:c.537C>G	ENSP00000340883.6:p.Asp179Glu
ENST00000407082.3:c.372C>G	ENSP00000385226.3:p.Asp124Glu
ENST00000407422.7:c.483C>G	ENSP00000383984.3:p.Asp161Glu
ENST00000417137.5:c.564C>G	ENSP00000388489.1:p.Asp188Glu
ENST00000634926.1:c.251C>G
ENST00000635578.1:c.224C>G
NM_001007468.1:c.483C>G	NP_001007469.1:p.Asp161Glu
NM_003073.3:c.510C>G , LRG_520t1:c.510C>G	NP_003064.2:p.Asp170Glu
XM_011530345.1:c.564C>G	XP_011528647.1:p.Asp188Glu
XM_011530346.1:c.537C>G	XP_011528648.1:p.Asp179Glu
NM_001007468.2:c.483C>G	NP_001007469.1:p.Asp161Glu
NM_001317946.1:c.537C>G	NP_001304875.1:p.Asp179Glu
NM_001362877.1:c.564C>G	NP_001349806.1:p.Asp188Glu
NM_003073.4:c.510C>G	NP_003064.2:p.Asp170Glu
NM_001007468.3:c.483C>G	NP_001007469.1:p.Asp161Glu
NM_001317946.2:c.537C>G	NP_001304875.1:p.Asp179Glu
NM_001362877.2:c.564C>G	NP_001349806.1:p.Asp188Glu
NM_003073.5:c.510C>G MANE Select	NP_003064.2:p.Asp170Glu