Canonical Allele Identifier: CA2655715129
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834382_23834384dup , CM000684.2:g.23834382_23834384dup GRCh38
NC_000022.10:g.24176569_24176571dup , CM000684.1:g.24176569_24176571dup GRCh37
NC_000022.9:g.22506569_22506571dup NCBI36
NG_009303.1:g.52420_52422dup , LRG_520:g.52420_52422dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*202_*204dup ENSP00000263121.8:n.*202_*204dup
ENST00000344921.11:c.*202_*204dup ENSP00000340883.6:n.*202_*204dup
ENST00000407422.8:c.*202_*204dup ENSP00000383984.3:n.*202_*204dup
ENST00000644036.2:c.*202_*204dup MANE Select ENSP00000494049.2:n.*202_*204dup
ENST00000647057.1:c.*854_*856dup ENSP00000494757.1:n.*854_*856dup
ENST00000263121.11:c.*202_*204dup ENSP00000263121.7:n.*202_*204dup
ENST00000344921.10:c.*202_*204dup ENSP00000340883.6:n.*202_*204dup
ENST00000407422.7:c.*202_*204dup ENSP00000383984.3:n.*202_*204dup
NM_001007468.1:c.*202_*204dup NP_001007469.1:n.*202_*204dup
NM_003073.3:c.*202_*204dup , LRG_520t1:c.*202_*204dup NP_003064.2:n.*202_*204dup
XM_011530345.1:c.*202_*204dup XP_011528647.1:n.*202_*204dup
XM_011530346.1:c.*202_*204dup XP_011528648.1:n.*202_*204dup
NM_001007468.2:c.*202_*204dup NP_001007469.1:n.*202_*204dup
NM_001317946.1:c.*202_*204dup NP_001304875.1:n.*202_*204dup
NM_001362877.1:c.*202_*204dup NP_001349806.1:n.*202_*204dup
NM_003073.4:c.*202_*204dup NP_003064.2:n.*202_*204dup
NM_001007468.3:c.*202_*204dup NP_001007469.1:n.*202_*204dup
NM_001317946.2:c.*202_*204dup NP_001304875.1:n.*202_*204dup
NM_001362877.2:c.*202_*204dup NP_001349806.1:n.*202_*204dup
NM_003073.5:c.*202_*204dup MANE Select NP_003064.2:n.*202_*204dup