Canonical Allele Identifier: CA2809468881

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628674T>C , CM000679.2:g.40628674T>C	GRCh38
NC_000017.10:g.38784926T>C , CM000679.1:g.38784926T>C	GRCh37
NC_000017.9:g.36038452T>C	NCBI36
NG_032163.1:g.24178A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*909A>G	ENSP00000466608.2:n.*909A>G
ENST00000348513.12:c.*111A>G MANE Select	ENSP00000323967.6:n.*111A>G
ENST00000377808.9:c.*334A>G	ENSP00000367039.4:n.*334A>G
ENST00000400122.8:c.*334A>G	ENSP00000411607.2:n.*334A>G
ENST00000469334.6:n.1945A>G
ENST00000578112.6:c.*1144A>G	ENSP00000464501.1:n.*1144A>G
ENST00000580419.6:c.*326A>G	ENSP00000462475.2:n.*326A>G
ENST00000642576.1:n.2490A>G
ENST00000643030.1:n.1970A>G
ENST00000643255.1:c.*3411A>G	ENSP00000493957.1:n.*3411A>G
ENST00000643318.1:c.*111A>G	ENSP00000494771.1:n.*111A>G
ENST00000643378.1:n.1902A>G
ENST00000643683.1:c.*111A>G	ENSP00000496094.1:n.*111A>G
ENST00000643893.1:n.1640A>G
ENST00000644443.1:n.3235A>G
ENST00000644523.1:n.1393A>G
ENST00000644527.1:c.*111A>G	ENSP00000493974.1:n.*111A>G
ENST00000644701.1:c.*334A>G	ENSP00000496097.1:n.*334A>G
ENST00000644909.1:c.*616A>G	ENSP00000493649.1:n.*616A>G
ENST00000645152.1:n.2010A>G
ENST00000645227.1:c.*1035A>G	ENSP00000495021.1:n.*1035A>G
ENST00000646242.1:n.7259A>G
ENST00000646283.1:c.*111A>G	ENSP00000494537.1:n.*111A>G
ENST00000646401.1:n.2713A>G
ENST00000646856.1:c.*1223A>G	ENSP00000494505.1:n.*1223A>G
ENST00000647294.1:c.*1277A>G	ENSP00000494815.1:n.*1277A>G
ENST00000647508.1:c.*111A>G	ENSP00000496445.1:n.*111A>G
ENST00000647515.1:c.*878A>G	ENSP00000495857.1:n.*878A>G
ENST00000348513.10:c.*111A>G	ENSP00000323967.6:n.*111A>G
ENST00000431889.6:c.*111A>G	ENSP00000445370.1:n.*111A>G
ENST00000469334.5:n.1934A>G
ENST00000578112.5:c.*1144A>G	ENSP00000464501.1:n.*1144A>G
NM_003079.4:c.*111A>G	NP_003070.3:n.*111A>G
NM_003079.5:c.*111A>G MANE Select	NP_003070.3:n.*111A>G