Canonical Allele Identifier: CA2259640386

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628482A= , CM000679.2:g.40628482A=	GRCh38
NC_000017.10:g.38784734A= , CM000679.1:g.38784734A=	GRCh37
NC_000017.9:g.36038260A=	NCBI36
NG_032163.1:g.24370T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1101T=	ENSP00000466608.2:n.*1101T=
ENST00000348513.12:c.*303T= MANE Select	ENSP00000323967.6:n.*303T=
ENST00000377808.9:c.*526T=	ENSP00000367039.4:n.*526T=
ENST00000400122.8:c.*526T=	ENSP00000411607.2:n.*526T=
ENST00000469334.6:n.2137T=
ENST00000578112.6:c.*1336T=	ENSP00000464501.1:n.*1336T=
ENST00000580419.6:c.*518T=	ENSP00000462475.2:n.*518T=
ENST00000642576.1:n.2682T=
ENST00000643030.1:n.2162T=
ENST00000643255.1:c.*3603T=	ENSP00000493957.1:n.*3603T=
ENST00000643318.1:c.*303T=	ENSP00000494771.1:n.*303T=
ENST00000643378.1:n.2094T=
ENST00000643683.1:c.*303T=	ENSP00000496094.1:n.*303T=
ENST00000643893.1:n.1832T=
ENST00000644443.1:n.3427T=
ENST00000644523.1:n.1585T=
ENST00000644527.1:c.*303T=	ENSP00000493974.1:n.*303T=
ENST00000644701.1:c.*526T=	ENSP00000496097.1:n.*526T=
ENST00000644909.1:c.*808T=	ENSP00000493649.1:n.*808T=
ENST00000645152.1:n.2202T=
ENST00000645227.1:c.*1227T=	ENSP00000495021.1:n.*1227T=
ENST00000646242.1:n.7451T=
ENST00000646283.1:c.*303T=	ENSP00000494537.1:n.*303T=
ENST00000646401.1:n.2905T=
ENST00000646856.1:c.*1415T=	ENSP00000494505.1:n.*1415T=
ENST00000647294.1:c.*1469T=	ENSP00000494815.1:n.*1469T=
ENST00000647508.1:c.*303T=	ENSP00000496445.1:n.*303T=
ENST00000647515.1:c.*1070T=	ENSP00000495857.1:n.*1070T=
ENST00000348513.10:c.*303T=	ENSP00000323967.6:n.*303T=
ENST00000431889.6:c.*303T=	ENSP00000445370.1:n.*303T=
ENST00000469334.5:n.2126T=
ENST00000578112.5:c.*1336T=	ENSP00000464501.1:n.*1336T=
NM_003079.4:c.*303T=	NP_003070.3:n.*303T=
NM_003079.5:c.*303T= MANE Select	NP_003070.3:n.*303T=