Canonical Allele Identifier: CA2259640391

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628501T= , CM000679.2:g.40628501T=	GRCh38
NC_000017.10:g.38784753T= , CM000679.1:g.38784753T=	GRCh37
NC_000017.9:g.36038279T=	NCBI36
NG_032163.1:g.24351A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1082A=	ENSP00000466608.2:n.*1082A=
ENST00000348513.12:c.*284A= MANE Select	ENSP00000323967.6:n.*284A=
ENST00000377808.9:c.*507A=	ENSP00000367039.4:n.*507A=
ENST00000400122.8:c.*507A=	ENSP00000411607.2:n.*507A=
ENST00000469334.6:n.2118A=
ENST00000578112.6:c.*1317A=	ENSP00000464501.1:n.*1317A=
ENST00000580419.6:c.*499A=	ENSP00000462475.2:n.*499A=
ENST00000642576.1:n.2663A=
ENST00000643030.1:n.2143A=
ENST00000643255.1:c.*3584A=	ENSP00000493957.1:n.*3584A=
ENST00000643318.1:c.*284A=	ENSP00000494771.1:n.*284A=
ENST00000643378.1:n.2075A=
ENST00000643683.1:c.*284A=	ENSP00000496094.1:n.*284A=
ENST00000643893.1:n.1813A=
ENST00000644443.1:n.3408A=
ENST00000644523.1:n.1566A=
ENST00000644527.1:c.*284A=	ENSP00000493974.1:n.*284A=
ENST00000644701.1:c.*507A=	ENSP00000496097.1:n.*507A=
ENST00000644909.1:c.*789A=	ENSP00000493649.1:n.*789A=
ENST00000645152.1:n.2183A=
ENST00000645227.1:c.*1208A=	ENSP00000495021.1:n.*1208A=
ENST00000646242.1:n.7432A=
ENST00000646283.1:c.*284A=	ENSP00000494537.1:n.*284A=
ENST00000646401.1:n.2886A=
ENST00000646856.1:c.*1396A=	ENSP00000494505.1:n.*1396A=
ENST00000647294.1:c.*1450A=	ENSP00000494815.1:n.*1450A=
ENST00000647508.1:c.*284A=	ENSP00000496445.1:n.*284A=
ENST00000647515.1:c.*1051A=	ENSP00000495857.1:n.*1051A=
ENST00000348513.10:c.*284A=	ENSP00000323967.6:n.*284A=
ENST00000431889.6:c.*284A=	ENSP00000445370.1:n.*284A=
ENST00000469334.5:n.2107A=
ENST00000578112.5:c.*1317A=	ENSP00000464501.1:n.*1317A=
NM_003079.4:c.*284A=	NP_003070.3:n.*284A=
NM_003079.5:c.*284A= MANE Select	NP_003070.3:n.*284A=