Canonical Allele Identifier: CA2259640481

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628752A= , CM000679.2:g.40628752A=	GRCh38
NC_000017.10:g.38785004A= , CM000679.1:g.38785004A=	GRCh37
NC_000017.9:g.36038530A=	NCBI36
NG_032163.1:g.24100T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*831T=	ENSP00000466608.2:n.*831T=
ENST00000348513.12:c.*33T= MANE Select	ENSP00000323967.6:n.*33T=
ENST00000377808.9:c.*256T=	ENSP00000367039.4:n.*256T=
ENST00000400122.8:c.*256T=	ENSP00000411607.2:n.*256T=
ENST00000469334.6:n.1867T=
ENST00000578112.6:c.*1066T=	ENSP00000464501.1:n.*1066T=
ENST00000580419.6:c.*248T=	ENSP00000462475.2:n.*248T=
ENST00000642576.1:n.2412T=
ENST00000643030.1:n.1892T=
ENST00000643255.1:c.*3333T=	ENSP00000493957.1:n.*3333T=
ENST00000643318.1:c.*33T=	ENSP00000494771.1:n.*33T=
ENST00000643378.1:n.1824T=
ENST00000643683.1:c.*33T=	ENSP00000496094.1:n.*33T=
ENST00000643893.1:n.1562T=
ENST00000644443.1:n.3157T=
ENST00000644523.1:n.1315T=
ENST00000644527.1:c.*33T=	ENSP00000493974.1:n.*33T=
ENST00000644701.1:c.*256T=	ENSP00000496097.1:n.*256T=
ENST00000644909.1:c.*538T=	ENSP00000493649.1:n.*538T=
ENST00000645152.1:n.1932T=
ENST00000645227.1:c.*957T=	ENSP00000495021.1:n.*957T=
ENST00000646242.1:n.7181T=
ENST00000646283.1:c.*33T=	ENSP00000494537.1:n.*33T=
ENST00000646401.1:n.2635T=
ENST00000646856.1:c.*1145T=	ENSP00000494505.1:n.*1145T=
ENST00000647294.1:c.*1199T=	ENSP00000494815.1:n.*1199T=
ENST00000647508.1:c.*33T=	ENSP00000496445.1:n.*33T=
ENST00000647515.1:c.*800T=	ENSP00000495857.1:n.*800T=
ENST00000348513.10:c.*33T=	ENSP00000323967.6:n.*33T=
ENST00000431889.6:c.*33T=	ENSP00000445370.1:n.*33T=
ENST00000469334.5:n.1856T=
ENST00000578112.5:c.*1066T=	ENSP00000464501.1:n.*1066T=
NM_003079.4:c.*33T=	NP_003070.3:n.*33T=
NM_003079.5:c.*33T= MANE Select	NP_003070.3:n.*33T=