Canonical Allele Identifier: CA2259640350
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628384G= , CM000679.2:g.40628384G= GRCh38
NC_000017.10:g.38784636G= , CM000679.1:g.38784636G= GRCh37
NC_000017.9:g.36038162G= NCBI36
NG_032163.1:g.24468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*1199C= ENSP00000466608.2:n.*1199C=
ENST00000348513.12:c.*401C= MANE Select ENSP00000323967.6:n.*401C=
ENST00000377808.9:c.*624C= ENSP00000367039.4:n.*624C=
ENST00000400122.8:c.*624C= ENSP00000411607.2:n.*624C=
ENST00000469334.6:n.2235C=
ENST00000578112.6:c.*1434C= ENSP00000464501.1:n.*1434C=
ENST00000580419.6:c.*616C= ENSP00000462475.2:n.*616C=
ENST00000642576.1:n.2780C=
ENST00000643030.1:n.2260C=
ENST00000643255.1:c.*3701C= ENSP00000493957.1:n.*3701C=
ENST00000643318.1:c.*401C= ENSP00000494771.1:n.*401C=
ENST00000643378.1:n.2192C=
ENST00000643683.1:c.*401C= ENSP00000496094.1:n.*401C=
ENST00000643893.1:n.1930C=
ENST00000644443.1:n.3525C=
ENST00000644523.1:n.1683C=
ENST00000644527.1:c.*401C= ENSP00000493974.1:n.*401C=
ENST00000644701.1:c.*624C= ENSP00000496097.1:n.*624C=
ENST00000644909.1:c.*906C= ENSP00000493649.1:n.*906C=
ENST00000645152.1:n.2300C=
ENST00000645227.1:c.*1325C= ENSP00000495021.1:n.*1325C=
ENST00000646242.1:n.7549C=
ENST00000646283.1:c.*401C= ENSP00000494537.1:n.*401C=
ENST00000646401.1:n.3003C=
ENST00000646856.1:c.*1513C= ENSP00000494505.1:n.*1513C=
ENST00000647294.1:c.*1567C= ENSP00000494815.1:n.*1567C=
ENST00000647508.1:c.*401C= ENSP00000496445.1:n.*401C=
ENST00000647515.1:c.*1168C= ENSP00000495857.1:n.*1168C=
ENST00000348513.10:c.*401C= ENSP00000323967.6:n.*401C=
ENST00000578112.5:c.*1434C= ENSP00000464501.1:n.*1434C=
NM_003079.4:c.*401C= NP_003070.3:n.*401C=
NM_003079.5:c.*401C= MANE Select NP_003070.3:n.*401C=