Canonical Allele Identifier: CA2259640462

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628716A= , CM000679.2:g.40628716A=	GRCh38
NC_000017.10:g.38784968A= , CM000679.1:g.38784968A=	GRCh37
NC_000017.9:g.36038494A=	NCBI36
NG_032163.1:g.24136T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*867T=	ENSP00000466608.2:n.*867T=
ENST00000348513.12:c.*69T= MANE Select	ENSP00000323967.6:n.*69T=
ENST00000377808.9:c.*292T=	ENSP00000367039.4:n.*292T=
ENST00000400122.8:c.*292T=	ENSP00000411607.2:n.*292T=
ENST00000469334.6:n.1903T=
ENST00000578112.6:c.*1102T=	ENSP00000464501.1:n.*1102T=
ENST00000580419.6:c.*284T=	ENSP00000462475.2:n.*284T=
ENST00000642576.1:n.2448T=
ENST00000643030.1:n.1928T=
ENST00000643255.1:c.*3369T=	ENSP00000493957.1:n.*3369T=
ENST00000643318.1:c.*69T=	ENSP00000494771.1:n.*69T=
ENST00000643378.1:n.1860T=
ENST00000643683.1:c.*69T=	ENSP00000496094.1:n.*69T=
ENST00000643893.1:n.1598T=
ENST00000644443.1:n.3193T=
ENST00000644523.1:n.1351T=
ENST00000644527.1:c.*69T=	ENSP00000493974.1:n.*69T=
ENST00000644701.1:c.*292T=	ENSP00000496097.1:n.*292T=
ENST00000644909.1:c.*574T=	ENSP00000493649.1:n.*574T=
ENST00000645152.1:n.1968T=
ENST00000645227.1:c.*993T=	ENSP00000495021.1:n.*993T=
ENST00000646242.1:n.7217T=
ENST00000646283.1:c.*69T=	ENSP00000494537.1:n.*69T=
ENST00000646401.1:n.2671T=
ENST00000646856.1:c.*1181T=	ENSP00000494505.1:n.*1181T=
ENST00000647294.1:c.*1235T=	ENSP00000494815.1:n.*1235T=
ENST00000647508.1:c.*69T=	ENSP00000496445.1:n.*69T=
ENST00000647515.1:c.*836T=	ENSP00000495857.1:n.*836T=
ENST00000348513.10:c.*69T=	ENSP00000323967.6:n.*69T=
ENST00000431889.6:c.*69T=	ENSP00000445370.1:n.*69T=
ENST00000469334.5:n.1892T=
ENST00000578112.5:c.*1102T=	ENSP00000464501.1:n.*1102T=
NM_003079.4:c.*69T=	NP_003070.3:n.*69T=
NM_003079.5:c.*69T= MANE Select	NP_003070.3:n.*69T=