Canonical Allele Identifier: CA645615107
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23803295_23803422del , CM000684.2:g.23803295_23803422del GRCh38
NC_000022.10:g.24145482_24145609del , CM000684.1:g.24145482_24145609del GRCh37
NC_000022.9:g.22475482_22475609del NCBI36
NG_009303.1:g.21333_21460del , LRG_520:g.21333_21460del

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.363_490del
ENST00000344921.11:c.528_655del
ENST00000407422.8:c.474_601del
ENST00000417137.6:c.555_682del
ENST00000642275.1:n.749_876del
ENST00000642727.1:c.667_794del
ENST00000643421.1:n.469_596del
ENST00000644036.2:c.501_628del
ENST00000644462.1:c.1219_1346del
ENST00000644467.1:n.1295_1422del
ENST00000644619.1:c.*568_*695del
ENST00000646723.1:n.2702_2829del
ENST00000646911.1:n.413_540del
ENST00000647057.1:c.232_*122del
ENST00000263121.11:c.501_628del
ENST00000344921.10:c.528_655del
ENST00000407082.3:c.363_490del
ENST00000407422.7:c.474_601del
ENST00000417137.5:c.555_682del
NM_001007468.1:c.474_601del
NM_003073.3:c.501_628del , LRG_520t1:c.501_628del
XM_011530345.1:c.555_682del
XM_011530346.1:c.528_655del
NM_001007468.2:c.474_601del
NM_001317946.1:c.528_655del
NM_001362877.1:c.555_682del
NM_003073.4:c.501_628del
NM_001007468.3:c.474_601del
NM_001317946.2:c.528_655del
NM_001362877.2:c.555_682del
NM_003073.5:c.501_628del