Canonical Allele Identifier: CA645615142

Gene: SMARCB1

Linked Data

• COSMIC: COSM29493

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23825226_23834181del , CM000684.2:g.23825226_23834181del	GRCh38
NC_000022.10:g.24167413_24176368del , CM000684.1:g.24167413_24176368del	GRCh37
NC_000022.9:g.22497413_22506368del	NCBI36
NG_009303.1:g.43264_52219del , LRG_520:g.43264_52219del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.659_*1del
ENST00000344921.11:c.824_*1del
ENST00000407422.8:c.770_*1del
ENST00000644036.2:c.797_*1del
ENST00000644462.1:c.1515_1877del
ENST00000645799.1:n.2119_2481del
ENST00000646723.1:n.3143_3505del
ENST00000647057.1:c.*291_*653del
ENST00000263121.11:c.797_*1del
ENST00000344921.10:c.824_*1del
ENST00000407082.3:c.659_*1del
ENST00000407422.7:c.770_*1del
NM_001007468.1:c.770_*1del
NM_003073.3:c.797_*1del , LRG_520t1:c.797_*1del
XM_011530345.1:c.851_*1del
XM_011530346.1:c.824_*1del
NM_001007468.2:c.770_*1del
NM_001317946.1:c.824_*1del
NM_001362877.1:c.851_*1del
NM_003073.4:c.797_*1del
NM_001007468.3:c.770_*1del
NM_001317946.2:c.824_*1del
NM_001362877.2:c.851_*1del
NM_003073.5:c.797_*1del