Canonical Allele Identifier: CA2259640353

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628392T= , CM000679.2:g.40628392T=	GRCh38
NC_000017.10:g.38784644T= , CM000679.1:g.38784644T=	GRCh37
NC_000017.9:g.36038170T=	NCBI36
NG_032163.1:g.24460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1191A=	ENSP00000466608.2:n.*1191A=
ENST00000348513.12:c.*393A= MANE Select	ENSP00000323967.6:n.*393A=
ENST00000377808.9:c.*616A=	ENSP00000367039.4:n.*616A=
ENST00000400122.8:c.*616A=	ENSP00000411607.2:n.*616A=
ENST00000469334.6:n.2227A=
ENST00000578112.6:c.*1426A=	ENSP00000464501.1:n.*1426A=
ENST00000580419.6:c.*608A=	ENSP00000462475.2:n.*608A=
ENST00000642576.1:n.2772A=
ENST00000643030.1:n.2252A=
ENST00000643255.1:c.*3693A=	ENSP00000493957.1:n.*3693A=
ENST00000643318.1:c.*393A=	ENSP00000494771.1:n.*393A=
ENST00000643378.1:n.2184A=
ENST00000643683.1:c.*393A=	ENSP00000496094.1:n.*393A=
ENST00000643893.1:n.1922A=
ENST00000644443.1:n.3517A=
ENST00000644523.1:n.1675A=
ENST00000644527.1:c.*393A=	ENSP00000493974.1:n.*393A=
ENST00000644701.1:c.*616A=	ENSP00000496097.1:n.*616A=
ENST00000644909.1:c.*898A=	ENSP00000493649.1:n.*898A=
ENST00000645152.1:n.2292A=
ENST00000645227.1:c.*1317A=	ENSP00000495021.1:n.*1317A=
ENST00000646242.1:n.7541A=
ENST00000646283.1:c.*393A=	ENSP00000494537.1:n.*393A=
ENST00000646401.1:n.2995A=
ENST00000646856.1:c.*1505A=	ENSP00000494505.1:n.*1505A=
ENST00000647294.1:c.*1559A=	ENSP00000494815.1:n.*1559A=
ENST00000647508.1:c.*393A=	ENSP00000496445.1:n.*393A=
ENST00000647515.1:c.*1160A=	ENSP00000495857.1:n.*1160A=
ENST00000348513.10:c.*393A=	ENSP00000323967.6:n.*393A=
ENST00000578112.5:c.*1426A=	ENSP00000464501.1:n.*1426A=
NM_003079.4:c.*393A=	NP_003070.3:n.*393A=
NM_003079.5:c.*393A= MANE Select	NP_003070.3:n.*393A=