Canonical Allele Identifier: CA2259640486
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628765C= , CM000679.2:g.40628765C= GRCh38
NC_000017.10:g.38785017C= , CM000679.1:g.38785017C= GRCh37
NC_000017.9:g.36038543C= NCBI36
NG_032163.1:g.24087G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*818G= ENSP00000466608.2:n.*818G=
ENST00000348513.12:c.*20G= MANE Select ENSP00000323967.6:n.*20G=
ENST00000377808.9:c.*243G= ENSP00000367039.4:n.*243G=
ENST00000400122.8:c.*243G= ENSP00000411607.2:n.*243G=
ENST00000469334.6:n.1854G=
ENST00000578112.6:c.*1053G= ENSP00000464501.1:n.*1053G=
ENST00000580419.6:c.*235G= ENSP00000462475.2:n.*235G=
ENST00000642576.1:n.2399G=
ENST00000643030.1:n.1879G=
ENST00000643255.1:c.*3320G= ENSP00000493957.1:n.*3320G=
ENST00000643318.1:c.*20G= ENSP00000494771.1:n.*20G=
ENST00000643378.1:n.1811G=
ENST00000643683.1:c.*20G= ENSP00000496094.1:n.*20G=
ENST00000643893.1:n.1549G=
ENST00000644443.1:n.3144G=
ENST00000644523.1:n.1302G=
ENST00000644527.1:c.*20G= ENSP00000493974.1:n.*20G=
ENST00000644701.1:c.*243G= ENSP00000496097.1:n.*243G=
ENST00000644909.1:c.*525G= ENSP00000493649.1:n.*525G=
ENST00000645152.1:n.1919G=
ENST00000645227.1:c.*944G= ENSP00000495021.1:n.*944G=
ENST00000646242.1:n.7168G=
ENST00000646283.1:c.*20G= ENSP00000494537.1:n.*20G=
ENST00000646401.1:n.2622G=
ENST00000646856.1:c.*1132G= ENSP00000494505.1:n.*1132G=
ENST00000647294.1:c.*1186G= ENSP00000494815.1:n.*1186G=
ENST00000647508.1:c.*20G= ENSP00000496445.1:n.*20G=
ENST00000647515.1:c.*787G= ENSP00000495857.1:n.*787G=
ENST00000348513.10:c.*20G= ENSP00000323967.6:n.*20G=
ENST00000431889.6:c.*20G= ENSP00000445370.1:n.*20G=
ENST00000469334.5:n.1843G=
ENST00000578112.5:c.*1053G= ENSP00000464501.1:n.*1053G=
NM_003079.4:c.*20G= NP_003070.3:n.*20G=
NM_003079.5:c.*20G= MANE Select NP_003070.3:n.*20G=