Canonical Allele Identifier: CA2259640413

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628567G= , CM000679.2:g.40628567G=	GRCh38
NC_000017.10:g.38784819G= , CM000679.1:g.38784819G=	GRCh37
NC_000017.9:g.36038345G=	NCBI36
NG_032163.1:g.24285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1016C=	ENSP00000466608.2:n.*1016C=
ENST00000348513.12:c.*218C= MANE Select	ENSP00000323967.6:n.*218C=
ENST00000377808.9:c.*441C=	ENSP00000367039.4:n.*441C=
ENST00000400122.8:c.*441C=	ENSP00000411607.2:n.*441C=
ENST00000469334.6:n.2052C=
ENST00000578112.6:c.*1251C=	ENSP00000464501.1:n.*1251C=
ENST00000580419.6:c.*433C=	ENSP00000462475.2:n.*433C=
ENST00000642576.1:n.2597C=
ENST00000643030.1:n.2077C=
ENST00000643255.1:c.*3518C=	ENSP00000493957.1:n.*3518C=
ENST00000643318.1:c.*218C=	ENSP00000494771.1:n.*218C=
ENST00000643378.1:n.2009C=
ENST00000643683.1:c.*218C=	ENSP00000496094.1:n.*218C=
ENST00000643893.1:n.1747C=
ENST00000644443.1:n.3342C=
ENST00000644523.1:n.1500C=
ENST00000644527.1:c.*218C=	ENSP00000493974.1:n.*218C=
ENST00000644701.1:c.*441C=	ENSP00000496097.1:n.*441C=
ENST00000644909.1:c.*723C=	ENSP00000493649.1:n.*723C=
ENST00000645152.1:n.2117C=
ENST00000645227.1:c.*1142C=	ENSP00000495021.1:n.*1142C=
ENST00000646242.1:n.7366C=
ENST00000646283.1:c.*218C=	ENSP00000494537.1:n.*218C=
ENST00000646401.1:n.2820C=
ENST00000646856.1:c.*1330C=	ENSP00000494505.1:n.*1330C=
ENST00000647294.1:c.*1384C=	ENSP00000494815.1:n.*1384C=
ENST00000647508.1:c.*218C=	ENSP00000496445.1:n.*218C=
ENST00000647515.1:c.*985C=	ENSP00000495857.1:n.*985C=
ENST00000348513.10:c.*218C=	ENSP00000323967.6:n.*218C=
ENST00000431889.6:c.*218C=	ENSP00000445370.1:n.*218C=
ENST00000469334.5:n.2041C=
ENST00000578112.5:c.*1251C=	ENSP00000464501.1:n.*1251C=
NM_003079.4:c.*218C=	NP_003070.3:n.*218C=
NM_003079.5:c.*218C= MANE Select	NP_003070.3:n.*218C=