Canonical Allele Identifier: CA2259640508
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628805C= , CM000679.2:g.40628805C= GRCh38
NC_000017.10:g.38785057C= , CM000679.1:g.38785057C= GRCh37
NC_000017.9:g.36038583C= NCBI36
NG_032163.1:g.24047G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*778G= ENSP00000466608.2:n.*778G=
ENST00000348513.12:c.1216G= MANE Select ENSP00000323967.6:p.Glu406=
ENST00000377808.9:c.*203G= ENSP00000367039.4:n.*203G=
ENST00000400122.8:c.*203G= ENSP00000411607.2:n.*203G=
ENST00000469334.6:n.1814G=
ENST00000578044.6:c.1006G= ENSP00000464511.1:p.Glu336=
ENST00000578112.6:c.*1013G= ENSP00000464501.1:n.*1013G=
ENST00000580419.6:c.*195G= ENSP00000462475.2:n.*195G=
ENST00000642576.1:n.2359G=
ENST00000643030.1:n.1839G=
ENST00000643255.1:c.*3280G= ENSP00000493957.1:n.*3280G=
ENST00000643318.1:c.1006G= ENSP00000494771.1:p.Glu336=
ENST00000643378.1:n.1771G=
ENST00000643683.1:c.1216G= ENSP00000496094.1:p.Glu406=
ENST00000643893.1:n.1509G=
ENST00000644443.1:n.3104G=
ENST00000644523.1:n.1262G=
ENST00000644527.1:c.988G= ENSP00000493974.1:p.Glu330=
ENST00000644701.1:c.*203G= ENSP00000496097.1:n.*203G=
ENST00000644909.1:c.*485G= ENSP00000493649.1:n.*485G=
ENST00000645152.1:n.1879G=
ENST00000645227.1:c.*904G= ENSP00000495021.1:n.*904G=
ENST00000646242.1:n.7128G=
ENST00000646283.1:c.1024G= ENSP00000494537.1:p.Glu342=
ENST00000646401.1:n.2582G=
ENST00000646448.1:n.2490G=
ENST00000646856.1:c.*1092G= ENSP00000494505.1:n.*1092G=
ENST00000647294.1:c.*1146G= ENSP00000494815.1:n.*1146G=
ENST00000647508.1:c.1111G= ENSP00000496445.1:p.Glu371=
ENST00000647515.1:c.*747G= ENSP00000495857.1:n.*747G=
ENST00000348513.10:c.1216G= ENSP00000323967.6:p.Glu406=
ENST00000377808.8:c.*203G= ENSP00000367039.4:n.*203G=
ENST00000400122.7:c.*203G= ENSP00000411607.2:n.*203G=
ENST00000431889.6:c.1162G= ENSP00000445370.1:p.Glu388=
ENST00000469334.5:n.1803G=
ENST00000476049.1:c.*1564G= ENSP00000463483.1:n.*1564G=
ENST00000578044.5:c.1006G= ENSP00000464511.1:p.Glu336=
ENST00000578112.5:c.*1013G= ENSP00000464501.1:n.*1013G=
ENST00000580419.5:c.1111G= ENSP00000462475.1:p.Glu371=
NM_003079.4:c.1216G= NP_003070.3:p.Glu406=
NM_003079.5:c.1216G= MANE Select NP_003070.3:p.Glu406=