Canonical Allele Identifier: CA2259640531
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628849C= , CM000679.2:g.40628849C= GRCh38
NC_000017.10:g.38785101C= , CM000679.1:g.38785101C= GRCh37
NC_000017.9:g.36038627C= NCBI36
NG_032163.1:g.24003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*734G= ENSP00000466608.2:n.*734G=
ENST00000348513.12:c.1172G= MANE Select ENSP00000323967.6:p.Ser391=
ENST00000377808.9:c.*159G= ENSP00000367039.4:n.*159G=
ENST00000400122.8:c.*159G= ENSP00000411607.2:n.*159G=
ENST00000469334.6:n.1770G=
ENST00000578044.6:c.962G= ENSP00000464511.1:p.Ser321=
ENST00000578112.6:c.*969G= ENSP00000464501.1:n.*969G=
ENST00000580419.6:c.*151G= ENSP00000462475.2:n.*151G=
ENST00000642576.1:n.2315G=
ENST00000643030.1:n.1795G=
ENST00000643255.1:c.*3236G= ENSP00000493957.1:n.*3236G=
ENST00000643318.1:c.962G= ENSP00000494771.1:p.Ser321=
ENST00000643378.1:n.1727G=
ENST00000643683.1:c.1172G= ENSP00000496094.1:p.Ser391=
ENST00000643893.1:n.1465G=
ENST00000644443.1:n.3060G=
ENST00000644523.1:n.1218G=
ENST00000644527.1:c.944G= ENSP00000493974.1:p.Ser315=
ENST00000644701.1:c.*159G= ENSP00000496097.1:n.*159G=
ENST00000644909.1:c.*441G= ENSP00000493649.1:n.*441G=
ENST00000645152.1:n.1835G=
ENST00000645227.1:c.*860G= ENSP00000495021.1:n.*860G=
ENST00000646242.1:n.7084G=
ENST00000646283.1:c.980G= ENSP00000494537.1:p.Ser327=
ENST00000646401.1:n.2538G=
ENST00000646448.1:n.2446G=
ENST00000646856.1:c.*1048G= ENSP00000494505.1:n.*1048G=
ENST00000647294.1:c.*1102G= ENSP00000494815.1:n.*1102G=
ENST00000647508.1:c.1067G= ENSP00000496445.1:p.Ser356=
ENST00000647515.1:c.*703G= ENSP00000495857.1:n.*703G=
ENST00000348513.10:c.1172G= ENSP00000323967.6:p.Ser391=
ENST00000377808.8:c.*159G= ENSP00000367039.4:n.*159G=
ENST00000400122.7:c.*159G= ENSP00000411607.2:n.*159G=
ENST00000431889.6:c.1118G= ENSP00000445370.1:p.Ser373=
ENST00000469334.5:n.1759G=
ENST00000476049.1:c.*1520G= ENSP00000463483.1:n.*1520G=
ENST00000578044.5:c.962G= ENSP00000464511.1:p.Ser321=
ENST00000578112.5:c.*969G= ENSP00000464501.1:n.*969G=
ENST00000580419.5:c.1067G= ENSP00000462475.1:p.Ser356=
NM_003079.4:c.1172G= NP_003070.3:p.Ser391=
NM_003079.5:c.1172G= MANE Select NP_003070.3:p.Ser391=