Canonical Allele Identifier: CA410933783
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23793619A>C , CM000684.2:g.23793619A>C GRCh38
NC_000022.10:g.24135806A>C , CM000684.1:g.24135806A>C GRCh37
NC_000022.9:g.22465806A>C NCBI36
NG_009303.1:g.11657A>C , LRG_520:g.11657A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.293A>C ENSP00000263121.8:p.Glu98Ala
ENST00000344921.11:c.266A>C ENSP00000340883.6:p.Glu89Ala
ENST00000407082.4:c.266A>C ENSP00000385226.4:p.Glu89Ala
ENST00000407422.8:c.266A>C ENSP00000383984.3:p.Glu89Ala
ENST00000417137.6:c.293A>C ENSP00000388489.2:p.Glu98Ala
ENST00000491967.2:n.456A>C
ENST00000643421.1:n.261A>C
ENST00000644036.2:c.293A>C MANE Select ENSP00000494049.2:p.Glu98Ala
ENST00000644462.1:c.128A>C ENSP00000494283.1:p.Glu43Ala
ENST00000644619.1:c.293A>C ENSP00000494695.1:p.Glu98Ala
ENST00000646421.1:n.2149A>C
ENST00000646723.1:n.281A>C
ENST00000646911.1:n.205A>C
ENST00000647057.1:c.93+6357A>C ENSP00000494757.1:n.93+6357A>C
ENST00000263121.11:c.293A>C ENSP00000263121.7:p.Glu98Ala
ENST00000344921.10:c.266A>C ENSP00000340883.6:p.Glu89Ala
ENST00000407082.3:c.293A>C ENSP00000385226.3:p.Glu98Ala
ENST00000407422.7:c.266A>C ENSP00000383984.3:p.Glu89Ala
ENST00000417137.5:c.293A>C ENSP00000388489.1:p.Glu98Ala
ENST00000491967.1:n.19A>C
ENST00000634926.1:c.145A>C
ENST00000635578.1:c.118A>C
NM_001007468.1:c.266A>C NP_001007469.1:p.Glu89Ala
NM_003073.3:c.293A>C , LRG_520t1:c.293A>C NP_003064.2:p.Glu98Ala
XM_011530345.1:c.293A>C XP_011528647.1:p.Glu98Ala
XM_011530346.1:c.266A>C XP_011528648.1:p.Glu89Ala
NM_001007468.2:c.266A>C NP_001007469.1:p.Glu89Ala
NM_001317946.1:c.266A>C NP_001304875.1:p.Glu89Ala
NM_001362877.1:c.293A>C NP_001349806.1:p.Glu98Ala
NM_003073.4:c.293A>C NP_003064.2:p.Glu98Ala
NM_001007468.3:c.266A>C NP_001007469.1:p.Glu89Ala
NM_001317946.2:c.266A>C NP_001304875.1:p.Glu89Ala
NM_001362877.2:c.293A>C NP_001349806.1:p.Glu98Ala
NM_003073.5:c.293A>C MANE Select NP_003064.2:p.Glu98Ala