Canonical Allele Identifier: CA656401653

Gene: SMARCE1

Linked Data

• COSMIC: COSN23302920

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628539dup , CM000679.2:g.40628539dup	GRCh38
NC_000017.10:g.38784791dup , CM000679.1:g.38784791dup	GRCh37
NC_000017.9:g.36038317dup	NCBI36
NG_032163.1:g.24313dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1044dup	ENSP00000466608.2:n.*1044dup
ENST00000348513.12:c.*246dup MANE Select	ENSP00000323967.6:n.*246dup
ENST00000377808.9:c.*469dup	ENSP00000367039.4:n.*469dup
ENST00000400122.8:c.*469dup	ENSP00000411607.2:n.*469dup
ENST00000469334.6:n.2080dup
ENST00000578112.6:c.*1279dup	ENSP00000464501.1:n.*1279dup
ENST00000580419.6:c.*461dup	ENSP00000462475.2:n.*461dup
ENST00000642576.1:n.2625dup
ENST00000643030.1:n.2105dup
ENST00000643255.1:c.*3546dup	ENSP00000493957.1:n.*3546dup
ENST00000643318.1:c.*246dup	ENSP00000494771.1:n.*246dup
ENST00000643378.1:n.2037dup
ENST00000643683.1:c.*246dup	ENSP00000496094.1:n.*246dup
ENST00000643893.1:n.1775dup
ENST00000644443.1:n.3370dup
ENST00000644523.1:n.1528dup
ENST00000644527.1:c.*246dup	ENSP00000493974.1:n.*246dup
ENST00000644701.1:c.*469dup	ENSP00000496097.1:n.*469dup
ENST00000644909.1:c.*751dup	ENSP00000493649.1:n.*751dup
ENST00000645152.1:n.2145dup
ENST00000645227.1:c.*1170dup	ENSP00000495021.1:n.*1170dup
ENST00000646242.1:n.7394dup
ENST00000646283.1:c.*246dup	ENSP00000494537.1:n.*246dup
ENST00000646401.1:n.2848dup
ENST00000646856.1:c.*1358dup	ENSP00000494505.1:n.*1358dup
ENST00000647294.1:c.*1412dup	ENSP00000494815.1:n.*1412dup
ENST00000647508.1:c.*246dup	ENSP00000496445.1:n.*246dup
ENST00000647515.1:c.*1013dup	ENSP00000495857.1:n.*1013dup
ENST00000348513.10:c.*246dup	ENSP00000323967.6:n.*246dup
ENST00000431889.6:c.*246dup	ENSP00000445370.1:n.*246dup
ENST00000469334.5:n.2069dup
ENST00000578112.5:c.*1279dup	ENSP00000464501.1:n.*1279dup
NM_003079.4:c.*246dup	NP_003070.3:n.*246dup
NM_003079.5:c.*246dup MANE Select	NP_003070.3:n.*246dup