Canonical Allele Identifier: CA2259640465

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628722T= , CM000679.2:g.40628722T=	GRCh38
NC_000017.10:g.38784974T= , CM000679.1:g.38784974T=	GRCh37
NC_000017.9:g.36038500T=	NCBI36
NG_032163.1:g.24130A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*861A=	ENSP00000466608.2:n.*861A=
ENST00000348513.12:c.*63A= MANE Select	ENSP00000323967.6:n.*63A=
ENST00000377808.9:c.*286A=	ENSP00000367039.4:n.*286A=
ENST00000400122.8:c.*286A=	ENSP00000411607.2:n.*286A=
ENST00000469334.6:n.1897A=
ENST00000578112.6:c.*1096A=	ENSP00000464501.1:n.*1096A=
ENST00000580419.6:c.*278A=	ENSP00000462475.2:n.*278A=
ENST00000642576.1:n.2442A=
ENST00000643030.1:n.1922A=
ENST00000643255.1:c.*3363A=	ENSP00000493957.1:n.*3363A=
ENST00000643318.1:c.*63A=	ENSP00000494771.1:n.*63A=
ENST00000643378.1:n.1854A=
ENST00000643683.1:c.*63A=	ENSP00000496094.1:n.*63A=
ENST00000643893.1:n.1592A=
ENST00000644443.1:n.3187A=
ENST00000644523.1:n.1345A=
ENST00000644527.1:c.*63A=	ENSP00000493974.1:n.*63A=
ENST00000644701.1:c.*286A=	ENSP00000496097.1:n.*286A=
ENST00000644909.1:c.*568A=	ENSP00000493649.1:n.*568A=
ENST00000645152.1:n.1962A=
ENST00000645227.1:c.*987A=	ENSP00000495021.1:n.*987A=
ENST00000646242.1:n.7211A=
ENST00000646283.1:c.*63A=	ENSP00000494537.1:n.*63A=
ENST00000646401.1:n.2665A=
ENST00000646856.1:c.*1175A=	ENSP00000494505.1:n.*1175A=
ENST00000647294.1:c.*1229A=	ENSP00000494815.1:n.*1229A=
ENST00000647508.1:c.*63A=	ENSP00000496445.1:n.*63A=
ENST00000647515.1:c.*830A=	ENSP00000495857.1:n.*830A=
ENST00000348513.10:c.*63A=	ENSP00000323967.6:n.*63A=
ENST00000431889.6:c.*63A=	ENSP00000445370.1:n.*63A=
ENST00000469334.5:n.1886A=
ENST00000578112.5:c.*1096A=	ENSP00000464501.1:n.*1096A=
NM_003079.4:c.*63A=	NP_003070.3:n.*63A=
NM_003079.5:c.*63A= MANE Select	NP_003070.3:n.*63A=