Canonical Allele Identifier: CA2576261821

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628754A>T , CM000679.2:g.40628754A>T	GRCh38
NC_000017.10:g.38785006A>T , CM000679.1:g.38785006A>T	GRCh37
NC_000017.9:g.36038532A>T	NCBI36
NG_032163.1:g.24098T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*829T>A	ENSP00000466608.2:n.*829T>A
ENST00000348513.12:c.*31T>A MANE Select	ENSP00000323967.6:n.*31T>A
ENST00000377808.9:c.*254T>A	ENSP00000367039.4:n.*254T>A
ENST00000400122.8:c.*254T>A	ENSP00000411607.2:n.*254T>A
ENST00000469334.6:n.1865T>A
ENST00000578112.6:c.*1064T>A	ENSP00000464501.1:n.*1064T>A
ENST00000580419.6:c.*246T>A	ENSP00000462475.2:n.*246T>A
ENST00000642576.1:n.2410T>A
ENST00000643030.1:n.1890T>A
ENST00000643255.1:c.*3331T>A	ENSP00000493957.1:n.*3331T>A
ENST00000643318.1:c.*31T>A	ENSP00000494771.1:n.*31T>A
ENST00000643378.1:n.1822T>A
ENST00000643683.1:c.*31T>A	ENSP00000496094.1:n.*31T>A
ENST00000643893.1:n.1560T>A
ENST00000644443.1:n.3155T>A
ENST00000644523.1:n.1313T>A
ENST00000644527.1:c.*31T>A	ENSP00000493974.1:n.*31T>A
ENST00000644701.1:c.*254T>A	ENSP00000496097.1:n.*254T>A
ENST00000644909.1:c.*536T>A	ENSP00000493649.1:n.*536T>A
ENST00000645152.1:n.1930T>A
ENST00000645227.1:c.*955T>A	ENSP00000495021.1:n.*955T>A
ENST00000646242.1:n.7179T>A
ENST00000646283.1:c.*31T>A	ENSP00000494537.1:n.*31T>A
ENST00000646401.1:n.2633T>A
ENST00000646856.1:c.*1143T>A	ENSP00000494505.1:n.*1143T>A
ENST00000647294.1:c.*1197T>A	ENSP00000494815.1:n.*1197T>A
ENST00000647508.1:c.*31T>A	ENSP00000496445.1:n.*31T>A
ENST00000647515.1:c.*798T>A	ENSP00000495857.1:n.*798T>A
ENST00000348513.10:c.*31T>A	ENSP00000323967.6:n.*31T>A
ENST00000431889.6:c.*31T>A	ENSP00000445370.1:n.*31T>A
ENST00000469334.5:n.1854T>A
ENST00000578112.5:c.*1064T>A	ENSP00000464501.1:n.*1064T>A
NM_003079.4:c.*31T>A	NP_003070.3:n.*31T>A
NM_003079.5:c.*31T>A MANE Select	NP_003070.3:n.*31T>A