Canonical Allele Identifier: CA2259640361
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628420G= , CM000679.2:g.40628420G= GRCh38
NC_000017.10:g.38784672G= , CM000679.1:g.38784672G= GRCh37
NC_000017.9:g.36038198G= NCBI36
NG_032163.1:g.24432C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*1163C= ENSP00000466608.2:n.*1163C=
ENST00000348513.12:c.*365C= MANE Select ENSP00000323967.6:n.*365C=
ENST00000377808.9:c.*588C= ENSP00000367039.4:n.*588C=
ENST00000400122.8:c.*588C= ENSP00000411607.2:n.*588C=
ENST00000469334.6:n.2199C=
ENST00000578112.6:c.*1398C= ENSP00000464501.1:n.*1398C=
ENST00000580419.6:c.*580C= ENSP00000462475.2:n.*580C=
ENST00000642576.1:n.2744C=
ENST00000643030.1:n.2224C=
ENST00000643255.1:c.*3665C= ENSP00000493957.1:n.*3665C=
ENST00000643318.1:c.*365C= ENSP00000494771.1:n.*365C=
ENST00000643378.1:n.2156C=
ENST00000643683.1:c.*365C= ENSP00000496094.1:n.*365C=
ENST00000643893.1:n.1894C=
ENST00000644443.1:n.3489C=
ENST00000644523.1:n.1647C=
ENST00000644527.1:c.*365C= ENSP00000493974.1:n.*365C=
ENST00000644701.1:c.*588C= ENSP00000496097.1:n.*588C=
ENST00000644909.1:c.*870C= ENSP00000493649.1:n.*870C=
ENST00000645152.1:n.2264C=
ENST00000645227.1:c.*1289C= ENSP00000495021.1:n.*1289C=
ENST00000646242.1:n.7513C=
ENST00000646283.1:c.*365C= ENSP00000494537.1:n.*365C=
ENST00000646401.1:n.2967C=
ENST00000646856.1:c.*1477C= ENSP00000494505.1:n.*1477C=
ENST00000647294.1:c.*1531C= ENSP00000494815.1:n.*1531C=
ENST00000647508.1:c.*365C= ENSP00000496445.1:n.*365C=
ENST00000647515.1:c.*1132C= ENSP00000495857.1:n.*1132C=
ENST00000348513.10:c.*365C= ENSP00000323967.6:n.*365C=
ENST00000578112.5:c.*1398C= ENSP00000464501.1:n.*1398C=
NM_003079.4:c.*365C= NP_003070.3:n.*365C=
NM_003079.5:c.*365C= MANE Select NP_003070.3:n.*365C=