Canonical Allele Identifier: CA2259640527

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628844T= , CM000679.2:g.40628844T=	GRCh38
NC_000017.10:g.38785096T= , CM000679.1:g.38785096T=	GRCh37
NC_000017.9:g.36038622T=	NCBI36
NG_032163.1:g.24008A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*739A=	ENSP00000466608.2:n.*739A=
ENST00000348513.12:c.1177A= MANE Select	ENSP00000323967.6:p.Ser393=
ENST00000377808.9:c.*164A=	ENSP00000367039.4:n.*164A=
ENST00000400122.8:c.*164A=	ENSP00000411607.2:n.*164A=
ENST00000469334.6:n.1775A=
ENST00000578044.6:c.967A=	ENSP00000464511.1:p.Ser323=
ENST00000578112.6:c.*974A=	ENSP00000464501.1:n.*974A=
ENST00000580419.6:c.*156A=	ENSP00000462475.2:n.*156A=
ENST00000642576.1:n.2320A=
ENST00000643030.1:n.1800A=
ENST00000643255.1:c.*3241A=	ENSP00000493957.1:n.*3241A=
ENST00000643318.1:c.967A=	ENSP00000494771.1:p.Ser323=
ENST00000643378.1:n.1732A=
ENST00000643683.1:c.1177A=	ENSP00000496094.1:p.Ser393=
ENST00000643893.1:n.1470A=
ENST00000644443.1:n.3065A=
ENST00000644523.1:n.1223A=
ENST00000644527.1:c.949A=	ENSP00000493974.1:p.Ser317=
ENST00000644701.1:c.*164A=	ENSP00000496097.1:n.*164A=
ENST00000644909.1:c.*446A=	ENSP00000493649.1:n.*446A=
ENST00000645152.1:n.1840A=
ENST00000645227.1:c.*865A=	ENSP00000495021.1:n.*865A=
ENST00000646242.1:n.7089A=
ENST00000646283.1:c.985A=	ENSP00000494537.1:p.Ser329=
ENST00000646401.1:n.2543A=
ENST00000646448.1:n.2451A=
ENST00000646856.1:c.*1053A=	ENSP00000494505.1:n.*1053A=
ENST00000647294.1:c.*1107A=	ENSP00000494815.1:n.*1107A=
ENST00000647508.1:c.1072A=	ENSP00000496445.1:p.Ser358=
ENST00000647515.1:c.*708A=	ENSP00000495857.1:n.*708A=
ENST00000348513.10:c.1177A=	ENSP00000323967.6:p.Ser393=
ENST00000377808.8:c.*164A=	ENSP00000367039.4:n.*164A=
ENST00000400122.7:c.*164A=	ENSP00000411607.2:n.*164A=
ENST00000431889.6:c.1123A=	ENSP00000445370.1:p.Ser375=
ENST00000469334.5:n.1764A=
ENST00000476049.1:c.*1525A=	ENSP00000463483.1:n.*1525A=
ENST00000578044.5:c.967A=	ENSP00000464511.1:p.Ser323=
ENST00000578112.5:c.*974A=	ENSP00000464501.1:n.*974A=
ENST00000580419.5:c.1072A=	ENSP00000462475.1:p.Ser358=
NM_003079.4:c.1177A=	NP_003070.3:p.Ser393=
NM_003079.5:c.1177A= MANE Select	NP_003070.3:p.Ser393=