Canonical Allele Identifier: CA2516151699
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834396_23834400del , CM000684.2:g.23834396_23834400del GRCh38
NC_000022.10:g.24176583_24176587del , CM000684.1:g.24176583_24176587del GRCh37
NC_000022.9:g.22506583_22506587del NCBI36
NG_009303.1:g.52434_52438del , LRG_520:g.52434_52438del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*216_*220del ENSP00000263121.8:n.*216_*220del
ENST00000344921.11:c.*216_*220del ENSP00000340883.6:n.*216_*220del
ENST00000407422.8:c.*216_*220del ENSP00000383984.3:n.*216_*220del
ENST00000644036.2:c.*216_*220del MANE Select ENSP00000494049.2:n.*216_*220del
ENST00000647057.1:c.*868_*872del ENSP00000494757.1:n.*868_*872del
ENST00000263121.11:c.*216_*220del ENSP00000263121.7:n.*216_*220del
ENST00000344921.10:c.*216_*220del ENSP00000340883.6:n.*216_*220del
ENST00000407422.7:c.*216_*220del ENSP00000383984.3:n.*216_*220del
NM_001007468.1:c.*216_*220del NP_001007469.1:n.*216_*220del
NM_003073.3:c.*216_*220del , LRG_520t1:c.*216_*220del NP_003064.2:n.*216_*220del
XM_011530345.1:c.*216_*220del XP_011528647.1:n.*216_*220del
XM_011530346.1:c.*216_*220del XP_011528648.1:n.*216_*220del
NM_001007468.2:c.*216_*220del NP_001007469.1:n.*216_*220del
NM_001317946.1:c.*216_*220del NP_001304875.1:n.*216_*220del
NM_001362877.1:c.*216_*220del NP_001349806.1:n.*216_*220del
NM_003073.4:c.*216_*220del NP_003064.2:n.*216_*220del
NM_001007468.3:c.*216_*220del NP_001007469.1:n.*216_*220del
NM_001317946.2:c.*216_*220del NP_001304875.1:n.*216_*220del
NM_001362877.2:c.*216_*220del NP_001349806.1:n.*216_*220del
NM_003073.5:c.*216_*220del MANE Select NP_003064.2:n.*216_*220del