Canonical Allele Identifier: CA2577663358
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834084_23834085insGC , CM000684.2:g.23834084_23834085insGC GRCh38
NC_000022.10:g.24176271_24176272insGC , CM000684.1:g.24176271_24176272insGC GRCh37
NC_000022.9:g.22506271_22506272insGC NCBI36
NG_009303.1:g.52122_52123insGC , LRG_520:g.52122_52123insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.981-57_981-56insGC ENSP00000263121.8:n.981-57_981-56insGC
ENST00000344921.11:c.1146-57_1146-56insGC ENSP00000340883.6:n.1146-57_1146-56insGC
ENST00000407422.8:c.1092-57_1092-56insGC ENSP00000383984.3:n.1092-57_1092-56insGC
ENST00000644036.2:c.1119-57_1119-56insGC MANE Select ENSP00000494049.2:n.1119-57_1119-56insGC
ENST00000644462.1:c.1837-57_1837-56insGC ENSP00000494283.1:n.1837-57_1837-56insGC
ENST00000645799.1:n.2441-57_2441-56insGC
ENST00000646723.1:n.3465-57_3465-56insGC
ENST00000647057.1:c.*613-57_*613-56insGC ENSP00000494757.1:n.*613-57_*613-56insGC
ENST00000263121.11:c.1119-57_1119-56insGC ENSP00000263121.7:n.1119-57_1119-56insGC
ENST00000344921.10:c.1146-57_1146-56insGC ENSP00000340883.6:n.1146-57_1146-56insGC
ENST00000407082.3:c.981-57_981-56insGC ENSP00000385226.3:n.981-57_981-56insGC
ENST00000407422.7:c.1092-57_1092-56insGC ENSP00000383984.3:n.1092-57_1092-56insGC
NM_001007468.1:c.1092-57_1092-56insGC NP_001007469.1:n.1092-57_1092-56insGC
NM_003073.3:c.1119-57_1119-56insGC , LRG_520t1:c.1119-57_1119-56insGC NP_003064.2:n.1119-57_1119-56insGC
XM_011530345.1:c.1173-57_1173-56insGC XP_011528647.1:n.1173-57_1173-56insGC
XM_011530346.1:c.1146-57_1146-56insGC XP_011528648.1:n.1146-57_1146-56insGC
NM_001007468.2:c.1092-57_1092-56insGC NP_001007469.1:n.1092-57_1092-56insGC
NM_001317946.1:c.1146-57_1146-56insGC NP_001304875.1:n.1146-57_1146-56insGC
NM_001362877.1:c.1173-57_1173-56insGC NP_001349806.1:n.1173-57_1173-56insGC
NM_003073.4:c.1119-57_1119-56insGC NP_003064.2:n.1119-57_1119-56insGC
NM_001007468.3:c.1092-57_1092-56insGC NP_001007469.1:n.1092-57_1092-56insGC
NM_001317946.2:c.1146-57_1146-56insGC NP_001304875.1:n.1146-57_1146-56insGC
NM_001362877.2:c.1173-57_1173-56insGC NP_001349806.1:n.1173-57_1173-56insGC
NM_003073.5:c.1119-57_1119-56insGC MANE Select NP_003064.2:n.1119-57_1119-56insGC