Canonical Allele Identifier: CA2259640346

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628378_40628380delinsAAG , CM000679.2:g.40628378_40628380delinsAAG	GRCh38
NC_000017.10:g.38784630_38784632delinsAAG , CM000679.1:g.38784630_38784632delinsAAG	GRCh37
NC_000017.9:g.36038156_36038158delinsAAG	NCBI36
NG_032163.1:g.24472_24474delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1203_*1205delinsCTT	ENSP00000466608.2:n.*1203_*1205delinsCTT
ENST00000348513.12:c.*405_*407delinsCTT MANE Select	ENSP00000323967.6:n.*405_*407delinsCTT
ENST00000377808.9:c.*628_*630delinsCTT	ENSP00000367039.4:n.*628_*630delinsCTT
ENST00000400122.8:c.*628_*630delinsCTT	ENSP00000411607.2:n.*628_*630delinsCTT
ENST00000469334.6:n.2239_2241delinsCTT
ENST00000578112.6:c.*1438_*1440delinsCTT	ENSP00000464501.1:n.*1438_*1440delinsCTT
ENST00000580419.6:c.*620_*622delinsCTT	ENSP00000462475.2:n.*620_*622delinsCTT
ENST00000642576.1:n.2784_2786delinsCTT
ENST00000643030.1:n.2264_2266delinsCTT
ENST00000643255.1:c.*3705_*3707delinsCTT	ENSP00000493957.1:n.*3705_*3707delinsCTT
ENST00000643318.1:c.*405_*407delinsCTT	ENSP00000494771.1:n.*405_*407delinsCTT
ENST00000643378.1:n.2196_2198delinsCTT
ENST00000643683.1:c.*405_*407delinsCTT	ENSP00000496094.1:n.*405_*407delinsCTT
ENST00000643893.1:n.1934_1936delinsCTT
ENST00000644443.1:n.3529_3531delinsCTT
ENST00000644523.1:n.1687_1689delinsCTT
ENST00000644527.1:c.*405_*407delinsCTT	ENSP00000493974.1:n.*405_*407delinsCTT
ENST00000644701.1:c.*628_*630delinsCTT	ENSP00000496097.1:n.*628_*630delinsCTT
ENST00000644909.1:c.*910_*912delinsCTT	ENSP00000493649.1:n.*910_*912delinsCTT
ENST00000645152.1:n.2304_2306delinsCTT
ENST00000645227.1:c.*1329_*1331delinsCTT	ENSP00000495021.1:n.*1329_*1331delinsCTT
ENST00000646242.1:n.7553_7555delinsCTT
ENST00000646283.1:c.*405_*407delinsCTT	ENSP00000494537.1:n.*405_*407delinsCTT
ENST00000646401.1:n.3007_3009delinsCTT
ENST00000646856.1:c.*1517_*1519delinsCTT	ENSP00000494505.1:n.*1517_*1519delinsCTT
ENST00000647294.1:c.*1571_*1573delinsCTT	ENSP00000494815.1:n.*1571_*1573delinsCTT
ENST00000647508.1:c.*405_*407delinsCTT	ENSP00000496445.1:n.*405_*407delinsCTT
ENST00000647515.1:c.*1172_*1174delinsCTT	ENSP00000495857.1:n.*1172_*1174delinsCTT
ENST00000348513.10:c.*405_*407delinsCTT	ENSP00000323967.6:n.*405_*407delinsCTT
ENST00000578112.5:c.*1438_*1440delinsCTT	ENSP00000464501.1:n.*1438_*1440delinsCTT
NM_003079.4:c.*405_*407delinsCTT	NP_003070.3:n.*405_*407delinsCTT
NM_003079.5:c.*405_*407delinsCTT MANE Select	NP_003070.3:n.*405_*407delinsCTT