Canonical Allele Identifier: CA2397980965
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23833644_23833646delinsGGA , CM000684.2:g.23833644_23833646delinsGGA GRCh38
NC_000022.10:g.24175831_24175833delinsGGA , CM000684.1:g.24175831_24175833delinsGGA GRCh37
NC_000022.9:g.22505831_22505833delinsGGA NCBI36
NG_009303.1:g.51682_51684delinsGGA , LRG_520:g.51682_51684delinsGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.921_923delinsGGA ENSP00000263121.8:p.Leu307=
ENST00000344921.11:c.1086_1088delinsGGA ENSP00000340883.6:p.Leu362=
ENST00000407422.8:c.1032_1034delinsGGA ENSP00000383984.3:p.Leu344=
ENST00000644036.2:c.1059_1061delinsGGA MANE Select ENSP00000494049.2:p.Leu353=
ENST00000644462.1:c.1777_1779delinsGGA ENSP00000494283.1:n.1777_1779delinsGGA
ENST00000645799.1:n.2381_2383delinsGGA
ENST00000646723.1:n.3405_3407delinsGGA
ENST00000647057.1:c.*553_*555delinsGGA ENSP00000494757.1:n.*553_*555delinsGGA
ENST00000263121.11:c.1059_1061delinsGGA ENSP00000263121.7:p.Leu353=
ENST00000344921.10:c.1086_1088delinsGGA ENSP00000340883.6:p.Leu362=
ENST00000407082.3:c.921_923delinsGGA ENSP00000385226.3:p.Leu307=
ENST00000407422.7:c.1032_1034delinsGGA ENSP00000383984.3:p.Leu344=
NM_001007468.1:c.1032_1034delinsGGA NP_001007469.1:p.Leu344=
NM_003073.3:c.1059_1061delinsGGA , LRG_520t1:c.1059_1061delinsGGA NP_003064.2:p.Leu353=
XM_011530345.1:c.1113_1115delinsGGA XP_011528647.1:p.Leu371=
XM_011530346.1:c.1086_1088delinsGGA XP_011528648.1:p.Leu362=
NM_001007468.2:c.1032_1034delinsGGA NP_001007469.1:p.Leu344=
NM_001317946.1:c.1086_1088delinsGGA NP_001304875.1:p.Leu362=
NM_001362877.1:c.1113_1115delinsGGA NP_001349806.1:p.Leu371=
NM_003073.4:c.1059_1061delinsGGA NP_003064.2:p.Leu353=
NM_001007468.3:c.1032_1034delinsGGA NP_001007469.1:p.Leu344=
NM_001317946.2:c.1086_1088delinsGGA NP_001304875.1:p.Leu362=
NM_001362877.2:c.1113_1115delinsGGA NP_001349806.1:p.Leu371=
NM_003073.5:c.1059_1061delinsGGA MANE Select NP_003064.2:p.Leu353=