Canonical Allele Identifier: CA2259640504
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628799C= , CM000679.2:g.40628799C= GRCh38
NC_000017.10:g.38785051C= , CM000679.1:g.38785051C= GRCh37
NC_000017.9:g.36038577C= NCBI36
NG_032163.1:g.24053G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*784G= ENSP00000466608.2:n.*784G=
ENST00000348513.12:c.1222G= MANE Select ENSP00000323967.6:p.Glu408=
ENST00000377808.9:c.*209G= ENSP00000367039.4:n.*209G=
ENST00000400122.8:c.*209G= ENSP00000411607.2:n.*209G=
ENST00000469334.6:n.1820G=
ENST00000578044.6:c.1012G= ENSP00000464511.1:p.Glu338=
ENST00000578112.6:c.*1019G= ENSP00000464501.1:n.*1019G=
ENST00000580419.6:c.*201G= ENSP00000462475.2:n.*201G=
ENST00000642576.1:n.2365G=
ENST00000643030.1:n.1845G=
ENST00000643255.1:c.*3286G= ENSP00000493957.1:n.*3286G=
ENST00000643318.1:c.1012G= ENSP00000494771.1:p.Glu338=
ENST00000643378.1:n.1777G=
ENST00000643683.1:c.1222G= ENSP00000496094.1:p.Glu408=
ENST00000643893.1:n.1515G=
ENST00000644443.1:n.3110G=
ENST00000644523.1:n.1268G=
ENST00000644527.1:c.994G= ENSP00000493974.1:p.Glu332=
ENST00000644701.1:c.*209G= ENSP00000496097.1:n.*209G=
ENST00000644909.1:c.*491G= ENSP00000493649.1:n.*491G=
ENST00000645152.1:n.1885G=
ENST00000645227.1:c.*910G= ENSP00000495021.1:n.*910G=
ENST00000646242.1:n.7134G=
ENST00000646283.1:c.1030G= ENSP00000494537.1:p.Glu344=
ENST00000646401.1:n.2588G=
ENST00000646448.1:n.2496G=
ENST00000646856.1:c.*1098G= ENSP00000494505.1:n.*1098G=
ENST00000647294.1:c.*1152G= ENSP00000494815.1:n.*1152G=
ENST00000647508.1:c.1117G= ENSP00000496445.1:p.Glu373=
ENST00000647515.1:c.*753G= ENSP00000495857.1:n.*753G=
ENST00000348513.10:c.1222G= ENSP00000323967.6:p.Glu408=
ENST00000377808.8:c.*209G= ENSP00000367039.4:n.*209G=
ENST00000400122.7:c.*209G= ENSP00000411607.2:n.*209G=
ENST00000431889.6:c.1168G= ENSP00000445370.1:p.Glu390=
ENST00000469334.5:n.1809G=
ENST00000476049.1:c.*1570G= ENSP00000463483.1:n.*1570G=
ENST00000578044.5:c.1012G= ENSP00000464511.1:p.Glu338=
ENST00000578112.5:c.*1019G= ENSP00000464501.1:n.*1019G=
ENST00000580419.5:c.1117G= ENSP00000462475.1:p.Glu373=
NM_003079.4:c.1222G= NP_003070.3:p.Glu408=
NM_003079.5:c.1222G= MANE Select NP_003070.3:p.Glu408=