Canonical Allele Identifier: CA2259640530
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628848G= , CM000679.2:g.40628848G= GRCh38
NC_000017.10:g.38785100G= , CM000679.1:g.38785100G= GRCh37
NC_000017.9:g.36038626G= NCBI36
NG_032163.1:g.24004C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*735C= ENSP00000466608.2:n.*735C=
ENST00000348513.12:c.1173C= MANE Select ENSP00000323967.6:p.Ser391=
ENST00000377808.9:c.*160C= ENSP00000367039.4:n.*160C=
ENST00000400122.8:c.*160C= ENSP00000411607.2:n.*160C=
ENST00000469334.6:n.1771C=
ENST00000578044.6:c.963C= ENSP00000464511.1:p.Ser321=
ENST00000578112.6:c.*970C= ENSP00000464501.1:n.*970C=
ENST00000580419.6:c.*152C= ENSP00000462475.2:n.*152C=
ENST00000642576.1:n.2316C=
ENST00000643030.1:n.1796C=
ENST00000643255.1:c.*3237C= ENSP00000493957.1:n.*3237C=
ENST00000643318.1:c.963C= ENSP00000494771.1:p.Ser321=
ENST00000643378.1:n.1728C=
ENST00000643683.1:c.1173C= ENSP00000496094.1:p.Ser391=
ENST00000643893.1:n.1466C=
ENST00000644443.1:n.3061C=
ENST00000644523.1:n.1219C=
ENST00000644527.1:c.945C= ENSP00000493974.1:p.Ser315=
ENST00000644701.1:c.*160C= ENSP00000496097.1:n.*160C=
ENST00000644909.1:c.*442C= ENSP00000493649.1:n.*442C=
ENST00000645152.1:n.1836C=
ENST00000645227.1:c.*861C= ENSP00000495021.1:n.*861C=
ENST00000646242.1:n.7085C=
ENST00000646283.1:c.981C= ENSP00000494537.1:p.Ser327=
ENST00000646401.1:n.2539C=
ENST00000646448.1:n.2447C=
ENST00000646856.1:c.*1049C= ENSP00000494505.1:n.*1049C=
ENST00000647294.1:c.*1103C= ENSP00000494815.1:n.*1103C=
ENST00000647508.1:c.1068C= ENSP00000496445.1:p.Ser356=
ENST00000647515.1:c.*704C= ENSP00000495857.1:n.*704C=
ENST00000348513.10:c.1173C= ENSP00000323967.6:p.Ser391=
ENST00000377808.8:c.*160C= ENSP00000367039.4:n.*160C=
ENST00000400122.7:c.*160C= ENSP00000411607.2:n.*160C=
ENST00000431889.6:c.1119C= ENSP00000445370.1:p.Ser373=
ENST00000469334.5:n.1760C=
ENST00000476049.1:c.*1521C= ENSP00000463483.1:n.*1521C=
ENST00000578044.5:c.963C= ENSP00000464511.1:p.Ser321=
ENST00000578112.5:c.*970C= ENSP00000464501.1:n.*970C=
ENST00000580419.5:c.1068C= ENSP00000462475.1:p.Ser356=
NM_003079.4:c.1173C= NP_003070.3:p.Ser391=
NM_003079.5:c.1173C= MANE Select NP_003070.3:p.Ser391=