Canonical Allele Identifier: CA2259640493
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628774C= , CM000679.2:g.40628774C= GRCh38
NC_000017.10:g.38785026C= , CM000679.1:g.38785026C= GRCh37
NC_000017.9:g.36038552C= NCBI36
NG_032163.1:g.24078G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*809G= ENSP00000466608.2:n.*809G=
ENST00000348513.12:c.*11G= MANE Select ENSP00000323967.6:n.*11G=
ENST00000377808.9:c.*234G= ENSP00000367039.4:n.*234G=
ENST00000400122.8:c.*234G= ENSP00000411607.2:n.*234G=
ENST00000469334.6:n.1845G=
ENST00000578112.6:c.*1044G= ENSP00000464501.1:n.*1044G=
ENST00000580419.6:c.*226G= ENSP00000462475.2:n.*226G=
ENST00000642576.1:n.2390G=
ENST00000643030.1:n.1870G=
ENST00000643255.1:c.*3311G= ENSP00000493957.1:n.*3311G=
ENST00000643318.1:c.*11G= ENSP00000494771.1:n.*11G=
ENST00000643378.1:n.1802G=
ENST00000643683.1:c.*11G= ENSP00000496094.1:n.*11G=
ENST00000643893.1:n.1540G=
ENST00000644443.1:n.3135G=
ENST00000644523.1:n.1293G=
ENST00000644527.1:c.*11G= ENSP00000493974.1:n.*11G=
ENST00000644701.1:c.*234G= ENSP00000496097.1:n.*234G=
ENST00000644909.1:c.*516G= ENSP00000493649.1:n.*516G=
ENST00000645152.1:n.1910G=
ENST00000645227.1:c.*935G= ENSP00000495021.1:n.*935G=
ENST00000646242.1:n.7159G=
ENST00000646283.1:c.*11G= ENSP00000494537.1:n.*11G=
ENST00000646401.1:n.2613G=
ENST00000646856.1:c.*1123G= ENSP00000494505.1:n.*1123G=
ENST00000647294.1:c.*1177G= ENSP00000494815.1:n.*1177G=
ENST00000647508.1:c.*11G= ENSP00000496445.1:n.*11G=
ENST00000647515.1:c.*778G= ENSP00000495857.1:n.*778G=
ENST00000348513.10:c.*11G= ENSP00000323967.6:n.*11G=
ENST00000431889.6:c.*11G= ENSP00000445370.1:n.*11G=
ENST00000469334.5:n.1834G=
ENST00000578112.5:c.*1044G= ENSP00000464501.1:n.*1044G=
NM_003079.4:c.*11G= NP_003070.3:n.*11G=
NM_003079.5:c.*11G= MANE Select NP_003070.3:n.*11G=