Canonical Allele Identifier: CA2259640371

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628456G= , CM000679.2:g.40628456G=	GRCh38
NC_000017.10:g.38784708G= , CM000679.1:g.38784708G=	GRCh37
NC_000017.9:g.36038234G=	NCBI36
NG_032163.1:g.24396C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1127C=	ENSP00000466608.2:n.*1127C=
ENST00000348513.12:c.*329C= MANE Select	ENSP00000323967.6:n.*329C=
ENST00000377808.9:c.*552C=	ENSP00000367039.4:n.*552C=
ENST00000400122.8:c.*552C=	ENSP00000411607.2:n.*552C=
ENST00000469334.6:n.2163C=
ENST00000578112.6:c.*1362C=	ENSP00000464501.1:n.*1362C=
ENST00000580419.6:c.*544C=	ENSP00000462475.2:n.*544C=
ENST00000642576.1:n.2708C=
ENST00000643030.1:n.2188C=
ENST00000643255.1:c.*3629C=	ENSP00000493957.1:n.*3629C=
ENST00000643318.1:c.*329C=	ENSP00000494771.1:n.*329C=
ENST00000643378.1:n.2120C=
ENST00000643683.1:c.*329C=	ENSP00000496094.1:n.*329C=
ENST00000643893.1:n.1858C=
ENST00000644443.1:n.3453C=
ENST00000644523.1:n.1611C=
ENST00000644527.1:c.*329C=	ENSP00000493974.1:n.*329C=
ENST00000644701.1:c.*552C=	ENSP00000496097.1:n.*552C=
ENST00000644909.1:c.*834C=	ENSP00000493649.1:n.*834C=
ENST00000645152.1:n.2228C=
ENST00000645227.1:c.*1253C=	ENSP00000495021.1:n.*1253C=
ENST00000646242.1:n.7477C=
ENST00000646283.1:c.*329C=	ENSP00000494537.1:n.*329C=
ENST00000646401.1:n.2931C=
ENST00000646856.1:c.*1441C=	ENSP00000494505.1:n.*1441C=
ENST00000647294.1:c.*1495C=	ENSP00000494815.1:n.*1495C=
ENST00000647508.1:c.*329C=	ENSP00000496445.1:n.*329C=
ENST00000647515.1:c.*1096C=	ENSP00000495857.1:n.*1096C=
ENST00000348513.10:c.*329C=	ENSP00000323967.6:n.*329C=
ENST00000578112.5:c.*1362C=	ENSP00000464501.1:n.*1362C=
NM_003079.4:c.*329C=	NP_003070.3:n.*329C=
NM_003079.5:c.*329C= MANE Select	NP_003070.3:n.*329C=