Canonical Allele Identifier: CA2259640430
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628630G= , CM000679.2:g.40628630G= GRCh38
NC_000017.10:g.38784882G= , CM000679.1:g.38784882G= GRCh37
NC_000017.9:g.36038408G= NCBI36
NG_032163.1:g.24222C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*953C= ENSP00000466608.2:n.*953C=
ENST00000348513.12:c.*155C= MANE Select ENSP00000323967.6:n.*155C=
ENST00000377808.9:c.*378C= ENSP00000367039.4:n.*378C=
ENST00000400122.8:c.*378C= ENSP00000411607.2:n.*378C=
ENST00000469334.6:n.1989C=
ENST00000578112.6:c.*1188C= ENSP00000464501.1:n.*1188C=
ENST00000580419.6:c.*370C= ENSP00000462475.2:n.*370C=
ENST00000642576.1:n.2534C=
ENST00000643030.1:n.2014C=
ENST00000643255.1:c.*3455C= ENSP00000493957.1:n.*3455C=
ENST00000643318.1:c.*155C= ENSP00000494771.1:n.*155C=
ENST00000643378.1:n.1946C=
ENST00000643683.1:c.*155C= ENSP00000496094.1:n.*155C=
ENST00000643893.1:n.1684C=
ENST00000644443.1:n.3279C=
ENST00000644523.1:n.1437C=
ENST00000644527.1:c.*155C= ENSP00000493974.1:n.*155C=
ENST00000644701.1:c.*378C= ENSP00000496097.1:n.*378C=
ENST00000644909.1:c.*660C= ENSP00000493649.1:n.*660C=
ENST00000645152.1:n.2054C=
ENST00000645227.1:c.*1079C= ENSP00000495021.1:n.*1079C=
ENST00000646242.1:n.7303C=
ENST00000646283.1:c.*155C= ENSP00000494537.1:n.*155C=
ENST00000646401.1:n.2757C=
ENST00000646856.1:c.*1267C= ENSP00000494505.1:n.*1267C=
ENST00000647294.1:c.*1321C= ENSP00000494815.1:n.*1321C=
ENST00000647508.1:c.*155C= ENSP00000496445.1:n.*155C=
ENST00000647515.1:c.*922C= ENSP00000495857.1:n.*922C=
ENST00000348513.10:c.*155C= ENSP00000323967.6:n.*155C=
ENST00000431889.6:c.*155C= ENSP00000445370.1:n.*155C=
ENST00000469334.5:n.1978C=
ENST00000578112.5:c.*1188C= ENSP00000464501.1:n.*1188C=
NM_003079.4:c.*155C= NP_003070.3:n.*155C=
NM_003079.5:c.*155C= MANE Select NP_003070.3:n.*155C=