Canonical Allele Identifier: CA2655715186
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834385_23834386insC , CM000684.2:g.23834385_23834386insC GRCh38
NC_000022.10:g.24176572_24176573insC , CM000684.1:g.24176572_24176573insC GRCh37
NC_000022.9:g.22506572_22506573insC NCBI36
NG_009303.1:g.52423_52424insC , LRG_520:g.52423_52424insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*205_*206insC ENSP00000263121.8:n.*205_*206insC
ENST00000344921.11:c.*205_*206insC ENSP00000340883.6:n.*205_*206insC
ENST00000407422.8:c.*205_*206insC ENSP00000383984.3:n.*205_*206insC
ENST00000644036.2:c.*205_*206insC MANE Select ENSP00000494049.2:n.*205_*206insC
ENST00000647057.1:c.*857_*858insC ENSP00000494757.1:n.*857_*858insC
ENST00000263121.11:c.*205_*206insC ENSP00000263121.7:n.*205_*206insC
ENST00000344921.10:c.*205_*206insC ENSP00000340883.6:n.*205_*206insC
ENST00000407422.7:c.*205_*206insC ENSP00000383984.3:n.*205_*206insC
NM_001007468.1:c.*205_*206insC NP_001007469.1:n.*205_*206insC
NM_003073.3:c.*205_*206insC , LRG_520t1:c.*205_*206insC NP_003064.2:n.*205_*206insC
XM_011530345.1:c.*205_*206insC XP_011528647.1:n.*205_*206insC
XM_011530346.1:c.*205_*206insC XP_011528648.1:n.*205_*206insC
NM_001007468.2:c.*205_*206insC NP_001007469.1:n.*205_*206insC
NM_001317946.1:c.*205_*206insC NP_001304875.1:n.*205_*206insC
NM_001362877.1:c.*205_*206insC NP_001349806.1:n.*205_*206insC
NM_003073.4:c.*205_*206insC NP_003064.2:n.*205_*206insC
NM_001007468.3:c.*205_*206insC NP_001007469.1:n.*205_*206insC
NM_001317946.2:c.*205_*206insC NP_001304875.1:n.*205_*206insC
NM_001362877.2:c.*205_*206insC NP_001349806.1:n.*205_*206insC
NM_003073.5:c.*205_*206insC MANE Select NP_003064.2:n.*205_*206insC