Canonical Allele Identifier: CA2259640533
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628852T= , CM000679.2:g.40628852T= GRCh38
NC_000017.10:g.38785104T= , CM000679.1:g.38785104T= GRCh37
NC_000017.9:g.36038630T= NCBI36
NG_032163.1:g.24000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*731A= ENSP00000466608.2:n.*731A=
ENST00000348513.12:c.1169A= MANE Select ENSP00000323967.6:p.Glu390=
ENST00000377808.9:c.*156A= ENSP00000367039.4:n.*156A=
ENST00000400122.8:c.*156A= ENSP00000411607.2:n.*156A=
ENST00000469334.6:n.1767A=
ENST00000578044.6:c.959A= ENSP00000464511.1:p.Glu320=
ENST00000578112.6:c.*966A= ENSP00000464501.1:n.*966A=
ENST00000580419.6:c.*148A= ENSP00000462475.2:n.*148A=
ENST00000642576.1:n.2312A=
ENST00000643030.1:n.1792A=
ENST00000643255.1:c.*3233A= ENSP00000493957.1:n.*3233A=
ENST00000643318.1:c.959A= ENSP00000494771.1:p.Glu320=
ENST00000643378.1:n.1724A=
ENST00000643683.1:c.1169A= ENSP00000496094.1:p.Glu390=
ENST00000643893.1:n.1462A=
ENST00000644443.1:n.3057A=
ENST00000644523.1:n.1215A=
ENST00000644527.1:c.941A= ENSP00000493974.1:p.Glu314=
ENST00000644701.1:c.*156A= ENSP00000496097.1:n.*156A=
ENST00000644909.1:c.*438A= ENSP00000493649.1:n.*438A=
ENST00000645152.1:n.1832A=
ENST00000645227.1:c.*857A= ENSP00000495021.1:n.*857A=
ENST00000646242.1:n.7081A=
ENST00000646283.1:c.977A= ENSP00000494537.1:p.Glu326=
ENST00000646401.1:n.2535A=
ENST00000646448.1:n.2443A=
ENST00000646856.1:c.*1045A= ENSP00000494505.1:n.*1045A=
ENST00000647294.1:c.*1099A= ENSP00000494815.1:n.*1099A=
ENST00000647508.1:c.1064A= ENSP00000496445.1:p.Glu355=
ENST00000647515.1:c.*700A= ENSP00000495857.1:n.*700A=
ENST00000348513.10:c.1169A= ENSP00000323967.6:p.Glu390=
ENST00000377808.8:c.*156A= ENSP00000367039.4:n.*156A=
ENST00000400122.7:c.*156A= ENSP00000411607.2:n.*156A=
ENST00000431889.6:c.1115A= ENSP00000445370.1:p.Glu372=
ENST00000469334.5:n.1756A=
ENST00000476049.1:c.*1517A= ENSP00000463483.1:n.*1517A=
ENST00000578044.5:c.959A= ENSP00000464511.1:p.Glu320=
ENST00000578112.5:c.*966A= ENSP00000464501.1:n.*966A=
ENST00000580419.5:c.1064A= ENSP00000462475.1:p.Glu355=
NM_003079.4:c.1169A= NP_003070.3:p.Glu390=
NM_003079.5:c.1169A= MANE Select NP_003070.3:p.Glu390=