Canonical Allele Identifier: CA2259640474

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628736C= , CM000679.2:g.40628736C=	GRCh38
NC_000017.10:g.38784988C= , CM000679.1:g.38784988C=	GRCh37
NC_000017.9:g.36038514C=	NCBI36
NG_032163.1:g.24116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*847G=	ENSP00000466608.2:n.*847G=
ENST00000348513.12:c.*49G= MANE Select	ENSP00000323967.6:n.*49G=
ENST00000377808.9:c.*272G=	ENSP00000367039.4:n.*272G=
ENST00000400122.8:c.*272G=	ENSP00000411607.2:n.*272G=
ENST00000469334.6:n.1883G=
ENST00000578112.6:c.*1082G=	ENSP00000464501.1:n.*1082G=
ENST00000580419.6:c.*264G=	ENSP00000462475.2:n.*264G=
ENST00000642576.1:n.2428G=
ENST00000643030.1:n.1908G=
ENST00000643255.1:c.*3349G=	ENSP00000493957.1:n.*3349G=
ENST00000643318.1:c.*49G=	ENSP00000494771.1:n.*49G=
ENST00000643378.1:n.1840G=
ENST00000643683.1:c.*49G=	ENSP00000496094.1:n.*49G=
ENST00000643893.1:n.1578G=
ENST00000644443.1:n.3173G=
ENST00000644523.1:n.1331G=
ENST00000644527.1:c.*49G=	ENSP00000493974.1:n.*49G=
ENST00000644701.1:c.*272G=	ENSP00000496097.1:n.*272G=
ENST00000644909.1:c.*554G=	ENSP00000493649.1:n.*554G=
ENST00000645152.1:n.1948G=
ENST00000645227.1:c.*973G=	ENSP00000495021.1:n.*973G=
ENST00000646242.1:n.7197G=
ENST00000646283.1:c.*49G=	ENSP00000494537.1:n.*49G=
ENST00000646401.1:n.2651G=
ENST00000646856.1:c.*1161G=	ENSP00000494505.1:n.*1161G=
ENST00000647294.1:c.*1215G=	ENSP00000494815.1:n.*1215G=
ENST00000647508.1:c.*49G=	ENSP00000496445.1:n.*49G=
ENST00000647515.1:c.*816G=	ENSP00000495857.1:n.*816G=
ENST00000348513.10:c.*49G=	ENSP00000323967.6:n.*49G=
ENST00000431889.6:c.*49G=	ENSP00000445370.1:n.*49G=
ENST00000469334.5:n.1872G=
ENST00000578112.5:c.*1082G=	ENSP00000464501.1:n.*1082G=
NM_003079.4:c.*49G=	NP_003070.3:n.*49G=
NM_003079.5:c.*49G= MANE Select	NP_003070.3:n.*49G=