Canonical Allele Identifier: CA2818530555
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834023dup , CM000684.2:g.23834023dup GRCh38
NC_000022.10:g.24176210dup , CM000684.1:g.24176210dup GRCh37
NC_000022.9:g.22506210dup NCBI36
NG_009303.1:g.52061dup , LRG_520:g.52061dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.981-118dup ENSP00000263121.8:n.981-118dup
ENST00000344921.11:c.1146-118dup ENSP00000340883.6:n.1146-118dup
ENST00000407422.8:c.1092-118dup ENSP00000383984.3:n.1092-118dup
ENST00000644036.2:c.1119-118dup MANE Select ENSP00000494049.2:n.1119-118dup
ENST00000644462.1:c.1837-118dup ENSP00000494283.1:n.1837-118dup
ENST00000645799.1:n.2441-118dup
ENST00000646723.1:n.3465-118dup
ENST00000647057.1:c.*613-118dup ENSP00000494757.1:n.*613-118dup
ENST00000263121.11:c.1119-118dup ENSP00000263121.7:n.1119-118dup
ENST00000344921.10:c.1146-118dup ENSP00000340883.6:n.1146-118dup
ENST00000407082.3:c.981-118dup ENSP00000385226.3:n.981-118dup
ENST00000407422.7:c.1092-118dup ENSP00000383984.3:n.1092-118dup
NM_001007468.1:c.1092-118dup NP_001007469.1:n.1092-118dup
NM_003073.3:c.1119-118dup , LRG_520t1:c.1119-118dup NP_003064.2:n.1119-118dup
XM_011530345.1:c.1173-118dup XP_011528647.1:n.1173-118dup
XM_011530346.1:c.1146-118dup XP_011528648.1:n.1146-118dup
NM_001007468.2:c.1092-118dup NP_001007469.1:n.1092-118dup
NM_001317946.1:c.1146-118dup NP_001304875.1:n.1146-118dup
NM_001362877.1:c.1173-118dup NP_001349806.1:n.1173-118dup
NM_003073.4:c.1119-118dup NP_003064.2:n.1119-118dup
NM_001007468.3:c.1092-118dup NP_001007469.1:n.1092-118dup
NM_001317946.2:c.1146-118dup NP_001304875.1:n.1146-118dup
NM_001362877.2:c.1173-118dup NP_001349806.1:n.1173-118dup
NM_003073.5:c.1119-118dup MANE Select NP_003064.2:n.1119-118dup