Canonical Allele Identifier: CA410913982
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23833692C>A , CM000684.2:g.23833692C>A GRCh38
NC_000022.10:g.24175879C>A , CM000684.1:g.24175879C>A GRCh37
NC_000022.9:g.22505879C>A NCBI36
NG_009303.1:g.51730C>A , LRG_520:g.51730C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.969C>A ENSP00000263121.8:p.Asp323Glu
ENST00000344921.11:c.1134C>A ENSP00000340883.6:p.Asp378Glu
ENST00000407422.8:c.1080C>A ENSP00000383984.3:p.Asp360Glu
ENST00000644036.2:c.1107C>A MANE Select ENSP00000494049.2:p.Asp369Glu
ENST00000644462.1:c.1825C>A ENSP00000494283.1:n.1825C>A
ENST00000645799.1:n.2429C>A
ENST00000646723.1:n.3453C>A
ENST00000647057.1:c.*601C>A ENSP00000494757.1:n.*601C>A
ENST00000263121.11:c.1107C>A ENSP00000263121.7:p.Asp369Glu
ENST00000344921.10:c.1134C>A ENSP00000340883.6:p.Asp378Glu
ENST00000407082.3:c.969C>A ENSP00000385226.3:p.Asp323Glu
ENST00000407422.7:c.1080C>A ENSP00000383984.3:p.Asp360Glu
NM_001007468.1:c.1080C>A NP_001007469.1:p.Asp360Glu
NM_003073.3:c.1107C>A , LRG_520t1:c.1107C>A NP_003064.2:p.Asp369Glu
XM_011530345.1:c.1161C>A XP_011528647.1:p.Asp387Glu
XM_011530346.1:c.1134C>A XP_011528648.1:p.Asp378Glu
NM_001007468.2:c.1080C>A NP_001007469.1:p.Asp360Glu
NM_001317946.1:c.1134C>A NP_001304875.1:p.Asp378Glu
NM_001362877.1:c.1161C>A NP_001349806.1:p.Asp387Glu
NM_003073.4:c.1107C>A NP_003064.2:p.Asp369Glu
NM_001007468.3:c.1080C>A NP_001007469.1:p.Asp360Glu
NM_001317946.2:c.1134C>A NP_001304875.1:p.Asp378Glu
NM_001362877.2:c.1161C>A NP_001349806.1:p.Asp387Glu
NM_003073.5:c.1107C>A MANE Select NP_003064.2:p.Asp369Glu