Canonical Allele Identifier: CA2397958038
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23786986_23787004delinsGGCGGCCTGGTCGTCGTCT , CM000684.2:g.23786986_23787004delinsGGCGGCCTGGTCGTCGTCT GRCh38
NC_000022.10:g.24129173_24129191delinsGGCGGCCTGGTCGTCGTCT , CM000684.1:g.24129173_24129191delinsGGCGGCCTGGTCGTCGTCT GRCh37
NC_000022.9:g.22459173_22459191delinsGGCGGCCTGGTCGTCGTCT NCBI36
NG_009303.1:g.5024_5042delinsGGCGGCCTGGTCGTCGTCT , LRG_520:g.5024_5042delinsGGCGGCCTGGTCGTCGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344921.11:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT ENSP00000340883.6:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
ENST00000407422.8:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT ENSP00000383984.3:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
ENST00000491967.2:n.7_25delinsGGCGGCCTGGTCGTCGTCT
ENST00000644036.2:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT MANE Select ENSP00000494049.2:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
ENST00000646421.1:n.9_27delinsGGCGGCCTGGTCGTCGTCT
ENST00000647057.1:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT ENSP00000494757.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
ENST00000263121.11:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT ENSP00000263121.7:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
ENST00000344921.10:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT ENSP00000340883.6:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
ENST00000417137.5:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT ENSP00000388489.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_001007468.1:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_001007469.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_003073.3:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT , LRG_520t1:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_003064.2:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
XM_011530345.1:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT XP_011528647.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
XM_011530346.1:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT XP_011528648.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_001007468.2:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_001007469.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_001317946.1:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_001304875.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_001362877.1:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_001349806.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_003073.4:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_003064.2:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_001007468.3:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_001007469.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_001317946.2:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_001304875.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_001362877.2:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT NP_001349806.1:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT
NM_003073.5:c.-184_-166delinsGGCGGCCTGGTCGTCGTCT MANE Select NP_003064.2:n.-184_-166delinsGGCGGCCTGGTCGTCGTCT