Canonical Allele Identifier: CA2259640568
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628918T= , CM000679.2:g.40628918T= GRCh38
NC_000017.10:g.38785170T= , CM000679.1:g.38785170T= GRCh37
NC_000017.9:g.36038696T= NCBI36
NG_032163.1:g.23934A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*665A= ENSP00000466608.2:n.*665A=
ENST00000348513.12:c.1103A= MANE Select ENSP00000323967.6:p.Glu368=
ENST00000377808.9:c.*90A= ENSP00000367039.4:n.*90A=
ENST00000400122.8:c.*90A= ENSP00000411607.2:n.*90A=
ENST00000469334.6:n.1701A=
ENST00000578044.6:c.893A= ENSP00000464511.1:p.Glu298=
ENST00000578112.6:c.*900A= ENSP00000464501.1:n.*900A=
ENST00000580419.6:c.*82A= ENSP00000462475.2:n.*82A=
ENST00000642576.1:n.2246A=
ENST00000643030.1:n.1726A=
ENST00000643255.1:c.*3167A= ENSP00000493957.1:n.*3167A=
ENST00000643318.1:c.893A= ENSP00000494771.1:p.Glu298=
ENST00000643378.1:n.1658A=
ENST00000643683.1:c.1103A= ENSP00000496094.1:p.Glu368=
ENST00000643893.1:n.1396A=
ENST00000644443.1:n.2991A=
ENST00000644523.1:n.1149A=
ENST00000644527.1:c.875A= ENSP00000493974.1:p.Glu292=
ENST00000644701.1:c.*90A= ENSP00000496097.1:n.*90A=
ENST00000644909.1:c.*372A= ENSP00000493649.1:n.*372A=
ENST00000645152.1:n.1766A=
ENST00000645227.1:c.*791A= ENSP00000495021.1:n.*791A=
ENST00000646242.1:n.7015A=
ENST00000646283.1:c.911A= ENSP00000494537.1:p.Glu304=
ENST00000646401.1:n.2469A=
ENST00000646448.1:n.2377A=
ENST00000646856.1:c.*979A= ENSP00000494505.1:n.*979A=
ENST00000647294.1:c.*1033A= ENSP00000494815.1:n.*1033A=
ENST00000647508.1:c.998A= ENSP00000496445.1:p.Glu333=
ENST00000647515.1:c.*634A= ENSP00000495857.1:n.*634A=
ENST00000348513.10:c.1103A= ENSP00000323967.6:p.Glu368=
ENST00000377808.8:c.*90A= ENSP00000367039.4:n.*90A=
ENST00000400122.7:c.*90A= ENSP00000411607.2:n.*90A=
ENST00000431889.6:c.1049A= ENSP00000445370.1:p.Glu350=
ENST00000469334.5:n.1690A=
ENST00000476049.1:c.*1451A= ENSP00000463483.1:n.*1451A=
ENST00000578044.5:c.893A= ENSP00000464511.1:p.Glu298=
ENST00000578112.5:c.*900A= ENSP00000464501.1:n.*900A=
ENST00000580419.5:c.998A= ENSP00000462475.1:p.Glu333=
NM_003079.4:c.1103A= NP_003070.3:p.Glu368=
NM_003079.5:c.1103A= MANE Select NP_003070.3:p.Glu368=