Canonical Allele Identifier: CA2655715312
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834395_23834396insCCCACCC , CM000684.2:g.23834395_23834396insCCCACCC GRCh38
NC_000022.10:g.24176582_24176583insCCCACCC , CM000684.1:g.24176582_24176583insCCCACCC GRCh37
NC_000022.9:g.22506582_22506583insCCCACCC NCBI36
NG_009303.1:g.52433_52434insCCCACCC , LRG_520:g.52433_52434insCCCACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*215_*216insCCCACCC ENSP00000263121.8:n.*215_*216insCCCACCC
ENST00000344921.11:c.*215_*216insCCCACCC ENSP00000340883.6:n.*215_*216insCCCACCC
ENST00000407422.8:c.*215_*216insCCCACCC ENSP00000383984.3:n.*215_*216insCCCACCC
ENST00000644036.2:c.*215_*216insCCCACCC MANE Select ENSP00000494049.2:n.*215_*216insCCCACCC
ENST00000647057.1:c.*867_*868insCCCACCC ENSP00000494757.1:n.*867_*868insCCCACCC
ENST00000263121.11:c.*215_*216insCCCACCC ENSP00000263121.7:n.*215_*216insCCCACCC
ENST00000344921.10:c.*215_*216insCCCACCC ENSP00000340883.6:n.*215_*216insCCCACCC
ENST00000407422.7:c.*215_*216insCCCACCC ENSP00000383984.3:n.*215_*216insCCCACCC
NM_001007468.1:c.*215_*216insCCCACCC NP_001007469.1:n.*215_*216insCCCACCC
NM_003073.3:c.*215_*216insCCCACCC , LRG_520t1:c.*215_*216insCCCACCC NP_003064.2:n.*215_*216insCCCACCC
XM_011530345.1:c.*215_*216insCCCACCC XP_011528647.1:n.*215_*216insCCCACCC
XM_011530346.1:c.*215_*216insCCCACCC XP_011528648.1:n.*215_*216insCCCACCC
NM_001007468.2:c.*215_*216insCCCACCC NP_001007469.1:n.*215_*216insCCCACCC
NM_001317946.1:c.*215_*216insCCCACCC NP_001304875.1:n.*215_*216insCCCACCC
NM_001362877.1:c.*215_*216insCCCACCC NP_001349806.1:n.*215_*216insCCCACCC
NM_003073.4:c.*215_*216insCCCACCC NP_003064.2:n.*215_*216insCCCACCC
NM_001007468.3:c.*215_*216insCCCACCC NP_001007469.1:n.*215_*216insCCCACCC
NM_001317946.2:c.*215_*216insCCCACCC NP_001304875.1:n.*215_*216insCCCACCC
NM_001362877.2:c.*215_*216insCCCACCC NP_001349806.1:n.*215_*216insCCCACCC
NM_003073.5:c.*215_*216insCCCACCC MANE Select NP_003064.2:n.*215_*216insCCCACCC