Canonical Allele Identifier: CA2733539363

Gene: SMARCE1

Linked Data

• dbSNP Id: rs2143980091

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628756T>A , CM000679.2:g.40628756T>A	GRCh38
NC_000017.10:g.38785008T>A , CM000679.1:g.38785008T>A	GRCh37
NC_000017.9:g.36038534T>A	NCBI36
NG_032163.1:g.24096A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*827A>T	ENSP00000466608.2:n.*827A>T
ENST00000348513.12:c.*29A>T MANE Select	ENSP00000323967.6:n.*29A>T
ENST00000377808.9:c.*252A>T	ENSP00000367039.4:n.*252A>T
ENST00000400122.8:c.*252A>T	ENSP00000411607.2:n.*252A>T
ENST00000469334.6:n.1863A>T
ENST00000578112.6:c.*1062A>T	ENSP00000464501.1:n.*1062A>T
ENST00000580419.6:c.*244A>T	ENSP00000462475.2:n.*244A>T
ENST00000642576.1:n.2408A>T
ENST00000643030.1:n.1888A>T
ENST00000643255.1:c.*3329A>T	ENSP00000493957.1:n.*3329A>T
ENST00000643318.1:c.*29A>T	ENSP00000494771.1:n.*29A>T
ENST00000643378.1:n.1820A>T
ENST00000643683.1:c.*29A>T	ENSP00000496094.1:n.*29A>T
ENST00000643893.1:n.1558A>T
ENST00000644443.1:n.3153A>T
ENST00000644523.1:n.1311A>T
ENST00000644527.1:c.*29A>T	ENSP00000493974.1:n.*29A>T
ENST00000644701.1:c.*252A>T	ENSP00000496097.1:n.*252A>T
ENST00000644909.1:c.*534A>T	ENSP00000493649.1:n.*534A>T
ENST00000645152.1:n.1928A>T
ENST00000645227.1:c.*953A>T	ENSP00000495021.1:n.*953A>T
ENST00000646242.1:n.7177A>T
ENST00000646283.1:c.*29A>T	ENSP00000494537.1:n.*29A>T
ENST00000646401.1:n.2631A>T
ENST00000646856.1:c.*1141A>T	ENSP00000494505.1:n.*1141A>T
ENST00000647294.1:c.*1195A>T	ENSP00000494815.1:n.*1195A>T
ENST00000647508.1:c.*29A>T	ENSP00000496445.1:n.*29A>T
ENST00000647515.1:c.*796A>T	ENSP00000495857.1:n.*796A>T
ENST00000348513.10:c.*29A>T	ENSP00000323967.6:n.*29A>T
ENST00000431889.6:c.*29A>T	ENSP00000445370.1:n.*29A>T
ENST00000469334.5:n.1852A>T
ENST00000578112.5:c.*1062A>T	ENSP00000464501.1:n.*1062A>T
NM_003079.4:c.*29A>T	NP_003070.3:n.*29A>T
NM_003079.5:c.*29A>T MANE Select	NP_003070.3:n.*29A>T