Canonical Allele Identifier: CA2259640502
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628795T= , CM000679.2:g.40628795T= GRCh38
NC_000017.10:g.38785047T= , CM000679.1:g.38785047T= GRCh37
NC_000017.9:g.36038573T= NCBI36
NG_032163.1:g.24057A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*788A= ENSP00000466608.2:n.*788A=
ENST00000348513.12:c.1226A= MANE Select ENSP00000323967.6:p.Lys409=
ENST00000377808.9:c.*213A= ENSP00000367039.4:n.*213A=
ENST00000400122.8:c.*213A= ENSP00000411607.2:n.*213A=
ENST00000469334.6:n.1824A=
ENST00000578044.6:c.1016A= ENSP00000464511.1:p.Lys339=
ENST00000578112.6:c.*1023A= ENSP00000464501.1:n.*1023A=
ENST00000580419.6:c.*205A= ENSP00000462475.2:n.*205A=
ENST00000642576.1:n.2369A=
ENST00000643030.1:n.1849A=
ENST00000643255.1:c.*3290A= ENSP00000493957.1:n.*3290A=
ENST00000643318.1:c.1016A= ENSP00000494771.1:p.Lys339=
ENST00000643378.1:n.1781A=
ENST00000643683.1:c.1226A= ENSP00000496094.1:p.Lys409=
ENST00000643893.1:n.1519A=
ENST00000644443.1:n.3114A=
ENST00000644523.1:n.1272A=
ENST00000644527.1:c.998A= ENSP00000493974.1:p.Lys333=
ENST00000644701.1:c.*213A= ENSP00000496097.1:n.*213A=
ENST00000644909.1:c.*495A= ENSP00000493649.1:n.*495A=
ENST00000645152.1:n.1889A=
ENST00000645227.1:c.*914A= ENSP00000495021.1:n.*914A=
ENST00000646242.1:n.7138A=
ENST00000646283.1:c.1034A= ENSP00000494537.1:p.Lys345=
ENST00000646401.1:n.2592A=
ENST00000646448.1:n.2500A=
ENST00000646856.1:c.*1102A= ENSP00000494505.1:n.*1102A=
ENST00000647294.1:c.*1156A= ENSP00000494815.1:n.*1156A=
ENST00000647508.1:c.1121A= ENSP00000496445.1:p.Lys374=
ENST00000647515.1:c.*757A= ENSP00000495857.1:n.*757A=
ENST00000348513.10:c.1226A= ENSP00000323967.6:p.Lys409=
ENST00000377808.8:c.*213A= ENSP00000367039.4:n.*213A=
ENST00000400122.7:c.*213A= ENSP00000411607.2:n.*213A=
ENST00000431889.6:c.1172A= ENSP00000445370.1:p.Lys391=
ENST00000469334.5:n.1813A=
ENST00000578044.5:c.1016A= ENSP00000464511.1:p.Lys339=
ENST00000578112.5:c.*1023A= ENSP00000464501.1:n.*1023A=
ENST00000580419.5:c.1121A= ENSP00000462475.1:p.Lys374=
NM_003079.4:c.1226A= NP_003070.3:p.Lys409=
NM_003079.5:c.1226A= MANE Select NP_003070.3:p.Lys409=