Canonical Allele Identifier: CA645615103
Gene: SMARCB1 HGNC NCBI

Linked Data

COSMIC: COSM13446

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23800945_23803423del , CM000684.2:g.23800945_23803423del GRCh38
NC_000022.10:g.24143132_24145610del , CM000684.1:g.24143132_24145610del GRCh37
NC_000022.9:g.22473132_22475610del NCBI36
NG_009303.1:g.18983_21461del , LRG_520:g.18983_21461del

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.363-2350_490+1del
ENST00000344921.11:c.337_655+1del
ENST00000407422.8:c.337_601+1del
ENST00000417137.6:c.364_682+1del
ENST00000643421.1:n.332_597del
ENST00000644036.2:c.364_628+1del
ENST00000644462.1:c.199_1346+1del
ENST00000644619.1:c.364_*695+1del
ENST00000646723.1:n.352_2829+1del
ENST00000646911.1:n.276_540+1del
ENST00000647057.1:c.95_*122+1del
ENST00000263121.11:c.364_628+1del
ENST00000344921.10:c.337_655+1del
ENST00000407082.3:c.363-2350_490+1del
ENST00000407422.7:c.337_601+1del
NM_001007468.1:c.337_601+1del
NM_003073.3:c.364_628+1del , LRG_520t1:c.364_628+1del
XM_011530345.1:c.364_682+1del
XM_011530346.1:c.337_655+1del
NM_001007468.2:c.337_601+1del
NM_001317946.1:c.337_655+1del
NM_001362877.1:c.364_682+1del
NM_003073.4:c.364_628+1del
NM_001007468.3:c.337_601+1del
NM_001317946.2:c.337_655+1del
NM_001362877.2:c.364_682+1del
NM_003073.5:c.364_628+1del