Canonical Allele Identifier: CA2259640416

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628581C= , CM000679.2:g.40628581C=	GRCh38
NC_000017.10:g.38784833C= , CM000679.1:g.38784833C=	GRCh37
NC_000017.9:g.36038359C=	NCBI36
NG_032163.1:g.24271G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1002G=	ENSP00000466608.2:n.*1002G=
ENST00000348513.12:c.*204G= MANE Select	ENSP00000323967.6:n.*204G=
ENST00000377808.9:c.*427G=	ENSP00000367039.4:n.*427G=
ENST00000400122.8:c.*427G=	ENSP00000411607.2:n.*427G=
ENST00000469334.6:n.2038G=
ENST00000578112.6:c.*1237G=	ENSP00000464501.1:n.*1237G=
ENST00000580419.6:c.*419G=	ENSP00000462475.2:n.*419G=
ENST00000642576.1:n.2583G=
ENST00000643030.1:n.2063G=
ENST00000643255.1:c.*3504G=	ENSP00000493957.1:n.*3504G=
ENST00000643318.1:c.*204G=	ENSP00000494771.1:n.*204G=
ENST00000643378.1:n.1995G=
ENST00000643683.1:c.*204G=	ENSP00000496094.1:n.*204G=
ENST00000643893.1:n.1733G=
ENST00000644443.1:n.3328G=
ENST00000644523.1:n.1486G=
ENST00000644527.1:c.*204G=	ENSP00000493974.1:n.*204G=
ENST00000644701.1:c.*427G=	ENSP00000496097.1:n.*427G=
ENST00000644909.1:c.*709G=	ENSP00000493649.1:n.*709G=
ENST00000645152.1:n.2103G=
ENST00000645227.1:c.*1128G=	ENSP00000495021.1:n.*1128G=
ENST00000646242.1:n.7352G=
ENST00000646283.1:c.*204G=	ENSP00000494537.1:n.*204G=
ENST00000646401.1:n.2806G=
ENST00000646856.1:c.*1316G=	ENSP00000494505.1:n.*1316G=
ENST00000647294.1:c.*1370G=	ENSP00000494815.1:n.*1370G=
ENST00000647508.1:c.*204G=	ENSP00000496445.1:n.*204G=
ENST00000647515.1:c.*971G=	ENSP00000495857.1:n.*971G=
ENST00000348513.10:c.*204G=	ENSP00000323967.6:n.*204G=
ENST00000431889.6:c.*204G=	ENSP00000445370.1:n.*204G=
ENST00000469334.5:n.2027G=
ENST00000578112.5:c.*1237G=	ENSP00000464501.1:n.*1237G=
NM_003079.4:c.*204G=	NP_003070.3:n.*204G=
NM_003079.5:c.*204G= MANE Select	NP_003070.3:n.*204G=