Canonical Allele Identifier: CA2259640378

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628471_40628472delinsTG , CM000679.2:g.40628471_40628472delinsTG	GRCh38
NC_000017.10:g.38784723_38784724delinsTG , CM000679.1:g.38784723_38784724delinsTG	GRCh37
NC_000017.9:g.36038249_36038250delinsTG	NCBI36
NG_032163.1:g.24380_24381delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1111_*1112delinsCA	ENSP00000466608.2:n.*1111_*1112delinsCA
ENST00000348513.12:c.*313_*314delinsCA MANE Select	ENSP00000323967.6:n.*313_*314delinsCA
ENST00000377808.9:c.*536_*537delinsCA	ENSP00000367039.4:n.*536_*537delinsCA
ENST00000400122.8:c.*536_*537delinsCA	ENSP00000411607.2:n.*536_*537delinsCA
ENST00000469334.6:n.2147_2148delinsCA
ENST00000578112.6:c.*1346_*1347delinsCA	ENSP00000464501.1:n.*1346_*1347delinsCA
ENST00000580419.6:c.*528_*529delinsCA	ENSP00000462475.2:n.*528_*529delinsCA
ENST00000642576.1:n.2692_2693delinsCA
ENST00000643030.1:n.2172_2173delinsCA
ENST00000643255.1:c.*3613_*3614delinsCA	ENSP00000493957.1:n.*3613_*3614delinsCA
ENST00000643318.1:c.*313_*314delinsCA	ENSP00000494771.1:n.*313_*314delinsCA
ENST00000643378.1:n.2104_2105delinsCA
ENST00000643683.1:c.*313_*314delinsCA	ENSP00000496094.1:n.*313_*314delinsCA
ENST00000643893.1:n.1842_1843delinsCA
ENST00000644443.1:n.3437_3438delinsCA
ENST00000644523.1:n.1595_1596delinsCA
ENST00000644527.1:c.*313_*314delinsCA	ENSP00000493974.1:n.*313_*314delinsCA
ENST00000644701.1:c.*536_*537delinsCA	ENSP00000496097.1:n.*536_*537delinsCA
ENST00000644909.1:c.*818_*819delinsCA	ENSP00000493649.1:n.*818_*819delinsCA
ENST00000645152.1:n.2212_2213delinsCA
ENST00000645227.1:c.*1237_*1238delinsCA	ENSP00000495021.1:n.*1237_*1238delinsCA
ENST00000646242.1:n.7461_7462delinsCA
ENST00000646283.1:c.*313_*314delinsCA	ENSP00000494537.1:n.*313_*314delinsCA
ENST00000646401.1:n.2915_2916delinsCA
ENST00000646856.1:c.*1425_*1426delinsCA	ENSP00000494505.1:n.*1425_*1426delinsCA
ENST00000647294.1:c.*1479_*1480delinsCA	ENSP00000494815.1:n.*1479_*1480delinsCA
ENST00000647508.1:c.*313_*314delinsCA	ENSP00000496445.1:n.*313_*314delinsCA
ENST00000647515.1:c.*1080_*1081delinsCA	ENSP00000495857.1:n.*1080_*1081delinsCA
ENST00000348513.10:c.*313_*314delinsCA	ENSP00000323967.6:n.*313_*314delinsCA
ENST00000431889.6:c.*313_*314delinsCA	ENSP00000445370.1:n.*313_*314delinsCA
ENST00000578112.5:c.*1346_*1347delinsCA	ENSP00000464501.1:n.*1346_*1347delinsCA
NM_003079.4:c.*313_*314delinsCA	NP_003070.3:n.*313_*314delinsCA
NM_003079.5:c.*313_*314delinsCA MANE Select	NP_003070.3:n.*313_*314delinsCA