Canonical Allele Identifier: CA2655715338
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834395_23834396insCCCCCTC , CM000684.2:g.23834395_23834396insCCCCCTC GRCh38
NC_000022.10:g.24176582_24176583insCCCCCTC , CM000684.1:g.24176582_24176583insCCCCCTC GRCh37
NC_000022.9:g.22506582_22506583insCCCCCTC NCBI36
NG_009303.1:g.52433_52434insCCCCCTC , LRG_520:g.52433_52434insCCCCCTC

Transcript Alleles

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