Canonical Allele Identifier: CA2577663378
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834252del , CM000684.2:g.23834252del GRCh38
NC_000022.10:g.24176439del , CM000684.1:g.24176439del GRCh37
NC_000022.9:g.22506439del NCBI36
NG_009303.1:g.52290del , LRG_520:g.52290del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*72del ENSP00000263121.8:n.*72del
ENST00000344921.11:c.*72del ENSP00000340883.6:n.*72del
ENST00000407422.8:c.*72del ENSP00000383984.3:n.*72del
ENST00000644036.2:c.*72del MANE Select ENSP00000494049.2:n.*72del
ENST00000644462.1:c.1948del ENSP00000494283.1:n.1948del
ENST00000645799.1:n.2552del
ENST00000646723.1:n.3576del
ENST00000647057.1:c.*724del ENSP00000494757.1:n.*724del
ENST00000263121.11:c.*72del ENSP00000263121.7:n.*72del
ENST00000344921.10:c.*72del ENSP00000340883.6:n.*72del
ENST00000407422.7:c.*72del ENSP00000383984.3:n.*72del
NM_001007468.1:c.*72del NP_001007469.1:n.*72del
NM_003073.3:c.*72del , LRG_520t1:c.*72del NP_003064.2:n.*72del
XM_011530345.1:c.*72del XP_011528647.1:n.*72del
XM_011530346.1:c.*72del XP_011528648.1:n.*72del
NM_001007468.2:c.*72del NP_001007469.1:n.*72del
NM_001317946.1:c.*72del NP_001304875.1:n.*72del
NM_001362877.1:c.*72del NP_001349806.1:n.*72del
NM_003073.4:c.*72del NP_003064.2:n.*72del
NM_001007468.3:c.*72del NP_001007469.1:n.*72del
NM_001317946.2:c.*72del NP_001304875.1:n.*72del
NM_001362877.2:c.*72del NP_001349806.1:n.*72del
NM_003073.5:c.*72del MANE Select NP_003064.2:n.*72del