Canonical Allele Identifier: CA2259640461
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628713G= , CM000679.2:g.40628713G= GRCh38
NC_000017.10:g.38784965G= , CM000679.1:g.38784965G= GRCh37
NC_000017.9:g.36038491G= NCBI36
NG_032163.1:g.24139C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*870C= ENSP00000466608.2:n.*870C=
ENST00000348513.12:c.*72C= MANE Select ENSP00000323967.6:n.*72C=
ENST00000377808.9:c.*295C= ENSP00000367039.4:n.*295C=
ENST00000400122.8:c.*295C= ENSP00000411607.2:n.*295C=
ENST00000469334.6:n.1906C=
ENST00000578112.6:c.*1105C= ENSP00000464501.1:n.*1105C=
ENST00000580419.6:c.*287C= ENSP00000462475.2:n.*287C=
ENST00000642576.1:n.2451C=
ENST00000643030.1:n.1931C=
ENST00000643255.1:c.*3372C= ENSP00000493957.1:n.*3372C=
ENST00000643318.1:c.*72C= ENSP00000494771.1:n.*72C=
ENST00000643378.1:n.1863C=
ENST00000643683.1:c.*72C= ENSP00000496094.1:n.*72C=
ENST00000643893.1:n.1601C=
ENST00000644443.1:n.3196C=
ENST00000644523.1:n.1354C=
ENST00000644527.1:c.*72C= ENSP00000493974.1:n.*72C=
ENST00000644701.1:c.*295C= ENSP00000496097.1:n.*295C=
ENST00000644909.1:c.*577C= ENSP00000493649.1:n.*577C=
ENST00000645152.1:n.1971C=
ENST00000645227.1:c.*996C= ENSP00000495021.1:n.*996C=
ENST00000646242.1:n.7220C=
ENST00000646283.1:c.*72C= ENSP00000494537.1:n.*72C=
ENST00000646401.1:n.2674C=
ENST00000646856.1:c.*1184C= ENSP00000494505.1:n.*1184C=
ENST00000647294.1:c.*1238C= ENSP00000494815.1:n.*1238C=
ENST00000647508.1:c.*72C= ENSP00000496445.1:n.*72C=
ENST00000647515.1:c.*839C= ENSP00000495857.1:n.*839C=
ENST00000348513.10:c.*72C= ENSP00000323967.6:n.*72C=
ENST00000431889.6:c.*72C= ENSP00000445370.1:n.*72C=
ENST00000469334.5:n.1895C=
ENST00000578112.5:c.*1105C= ENSP00000464501.1:n.*1105C=
NM_003079.4:c.*72C= NP_003070.3:n.*72C=
NM_003079.5:c.*72C= MANE Select NP_003070.3:n.*72C=