Canonical Allele Identifier: CA920343780
Gene: SMARCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1568932936

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23787004_23787005insCCG , CM000684.2:g.23787004_23787005insCCG GRCh38
NC_000022.10:g.24129191_24129192insCCG , CM000684.1:g.24129191_24129192insCCG GRCh37
NC_000022.9:g.22459191_22459192insCCG NCBI36
NG_009303.1:g.5042_5043insCCG , LRG_520:g.5042_5043insCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000344921.11:c.-166_-165insCCG ENSP00000340883.6:n.-166_-165insCCG
ENST00000407422.8:c.-166_-165insCCG ENSP00000383984.3:n.-166_-165insCCG
ENST00000491967.2:n.25_26insCCG
ENST00000644036.2:c.-166_-165insCCG MANE Select ENSP00000494049.2:n.-166_-165insCCG
ENST00000644619.1:c.-166_-165insCCG ENSP00000494695.1:n.-166_-165insCCG
ENST00000646421.1:n.27_28insCCG
ENST00000647057.1:c.-166_-165insCCG ENSP00000494757.1:n.-166_-165insCCG
ENST00000263121.11:c.-166_-165insCCG ENSP00000263121.7:n.-166_-165insCCG
ENST00000344921.10:c.-166_-165insCCG ENSP00000340883.6:n.-166_-165insCCG
ENST00000407422.7:c.-166_-165insCCG ENSP00000383984.3:n.-166_-165insCCG
ENST00000417137.5:c.-166_-165insCCG ENSP00000388489.1:n.-166_-165insCCG
NM_001007468.1:c.-166_-165insCCG NP_001007469.1:n.-166_-165insCCG
NM_003073.3:c.-166_-165insCCG , LRG_520t1:c.-166_-165insCCG NP_003064.2:n.-166_-165insCCG
XM_011530345.1:c.-166_-165insCCG XP_011528647.1:n.-166_-165insCCG
XM_011530346.1:c.-166_-165insCCG XP_011528648.1:n.-166_-165insCCG
NM_001007468.2:c.-166_-165insCCG NP_001007469.1:n.-166_-165insCCG
NM_001317946.1:c.-166_-165insCCG NP_001304875.1:n.-166_-165insCCG
NM_001362877.1:c.-166_-165insCCG NP_001349806.1:n.-166_-165insCCG
NM_003073.4:c.-166_-165insCCG NP_003064.2:n.-166_-165insCCG
NM_001007468.3:c.-166_-165insCCG NP_001007469.1:n.-166_-165insCCG
NM_001317946.2:c.-166_-165insCCG NP_001304875.1:n.-166_-165insCCG
NM_001362877.2:c.-166_-165insCCG NP_001349806.1:n.-166_-165insCCG
NM_003073.5:c.-166_-165insCCG MANE Select NP_003064.2:n.-166_-165insCCG