Canonical Allele Identifier: CA2259640394

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628520G= , CM000679.2:g.40628520G=	GRCh38
NC_000017.10:g.38784772G= , CM000679.1:g.38784772G=	GRCh37
NC_000017.9:g.36038298G=	NCBI36
NG_032163.1:g.24332C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1063C=	ENSP00000466608.2:n.*1063C=
ENST00000348513.12:c.*265C= MANE Select	ENSP00000323967.6:n.*265C=
ENST00000377808.9:c.*488C=	ENSP00000367039.4:n.*488C=
ENST00000400122.8:c.*488C=	ENSP00000411607.2:n.*488C=
ENST00000469334.6:n.2099C=
ENST00000578112.6:c.*1298C=	ENSP00000464501.1:n.*1298C=
ENST00000580419.6:c.*480C=	ENSP00000462475.2:n.*480C=
ENST00000642576.1:n.2644C=
ENST00000643030.1:n.2124C=
ENST00000643255.1:c.*3565C=	ENSP00000493957.1:n.*3565C=
ENST00000643318.1:c.*265C=	ENSP00000494771.1:n.*265C=
ENST00000643378.1:n.2056C=
ENST00000643683.1:c.*265C=	ENSP00000496094.1:n.*265C=
ENST00000643893.1:n.1794C=
ENST00000644443.1:n.3389C=
ENST00000644523.1:n.1547C=
ENST00000644527.1:c.*265C=	ENSP00000493974.1:n.*265C=
ENST00000644701.1:c.*488C=	ENSP00000496097.1:n.*488C=
ENST00000644909.1:c.*770C=	ENSP00000493649.1:n.*770C=
ENST00000645152.1:n.2164C=
ENST00000645227.1:c.*1189C=	ENSP00000495021.1:n.*1189C=
ENST00000646242.1:n.7413C=
ENST00000646283.1:c.*265C=	ENSP00000494537.1:n.*265C=
ENST00000646401.1:n.2867C=
ENST00000646856.1:c.*1377C=	ENSP00000494505.1:n.*1377C=
ENST00000647294.1:c.*1431C=	ENSP00000494815.1:n.*1431C=
ENST00000647508.1:c.*265C=	ENSP00000496445.1:n.*265C=
ENST00000647515.1:c.*1032C=	ENSP00000495857.1:n.*1032C=
ENST00000348513.10:c.*265C=	ENSP00000323967.6:n.*265C=
ENST00000431889.6:c.*265C=	ENSP00000445370.1:n.*265C=
ENST00000469334.5:n.2088C=
ENST00000578112.5:c.*1298C=	ENSP00000464501.1:n.*1298C=
NM_003079.4:c.*265C=	NP_003070.3:n.*265C=
NM_003079.5:c.*265C= MANE Select	NP_003070.3:n.*265C=