Canonical Allele Identifier: CA2836824757

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628532A>G , CM000679.2:g.40628532A>G	GRCh38
NC_000017.10:g.38784784A>G , CM000679.1:g.38784784A>G	GRCh37
NC_000017.9:g.36038310A>G	NCBI36
NG_032163.1:g.24320T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1051T>C	ENSP00000466608.2:n.*1051T>C
ENST00000348513.12:c.*253T>C MANE Select	ENSP00000323967.6:n.*253T>C
ENST00000377808.9:c.*476T>C	ENSP00000367039.4:n.*476T>C
ENST00000400122.8:c.*476T>C	ENSP00000411607.2:n.*476T>C
ENST00000469334.6:n.2087T>C
ENST00000578112.6:c.*1286T>C	ENSP00000464501.1:n.*1286T>C
ENST00000580419.6:c.*468T>C	ENSP00000462475.2:n.*468T>C
ENST00000642576.1:n.2632T>C
ENST00000643030.1:n.2112T>C
ENST00000643255.1:c.*3553T>C	ENSP00000493957.1:n.*3553T>C
ENST00000643318.1:c.*253T>C	ENSP00000494771.1:n.*253T>C
ENST00000643378.1:n.2044T>C
ENST00000643683.1:c.*253T>C	ENSP00000496094.1:n.*253T>C
ENST00000643893.1:n.1782T>C
ENST00000644443.1:n.3377T>C
ENST00000644523.1:n.1535T>C
ENST00000644527.1:c.*253T>C	ENSP00000493974.1:n.*253T>C
ENST00000644701.1:c.*476T>C	ENSP00000496097.1:n.*476T>C
ENST00000644909.1:c.*758T>C	ENSP00000493649.1:n.*758T>C
ENST00000645152.1:n.2152T>C
ENST00000645227.1:c.*1177T>C	ENSP00000495021.1:n.*1177T>C
ENST00000646242.1:n.7401T>C
ENST00000646283.1:c.*253T>C	ENSP00000494537.1:n.*253T>C
ENST00000646401.1:n.2855T>C
ENST00000646856.1:c.*1365T>C	ENSP00000494505.1:n.*1365T>C
ENST00000647294.1:c.*1419T>C	ENSP00000494815.1:n.*1419T>C
ENST00000647508.1:c.*253T>C	ENSP00000496445.1:n.*253T>C
ENST00000647515.1:c.*1020T>C	ENSP00000495857.1:n.*1020T>C
ENST00000348513.10:c.*253T>C	ENSP00000323967.6:n.*253T>C
ENST00000431889.6:c.*253T>C	ENSP00000445370.1:n.*253T>C
ENST00000469334.5:n.2076T>C
ENST00000578112.5:c.*1286T>C	ENSP00000464501.1:n.*1286T>C
NM_003079.4:c.*253T>C	NP_003070.3:n.*253T>C
NM_003079.5:c.*253T>C MANE Select	NP_003070.3:n.*253T>C