Canonical Allele Identifier: CA2259640489
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628771A= , CM000679.2:g.40628771A= GRCh38
NC_000017.10:g.38785023A= , CM000679.1:g.38785023A= GRCh37
NC_000017.9:g.36038549A= NCBI36
NG_032163.1:g.24081T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*812T= ENSP00000466608.2:n.*812T=
ENST00000348513.12:c.*14T= MANE Select ENSP00000323967.6:n.*14T=
ENST00000377808.9:c.*237T= ENSP00000367039.4:n.*237T=
ENST00000400122.8:c.*237T= ENSP00000411607.2:n.*237T=
ENST00000469334.6:n.1848T=
ENST00000578112.6:c.*1047T= ENSP00000464501.1:n.*1047T=
ENST00000580419.6:c.*229T= ENSP00000462475.2:n.*229T=
ENST00000642576.1:n.2393T=
ENST00000643030.1:n.1873T=
ENST00000643255.1:c.*3314T= ENSP00000493957.1:n.*3314T=
ENST00000643318.1:c.*14T= ENSP00000494771.1:n.*14T=
ENST00000643378.1:n.1805T=
ENST00000643683.1:c.*14T= ENSP00000496094.1:n.*14T=
ENST00000643893.1:n.1543T=
ENST00000644443.1:n.3138T=
ENST00000644523.1:n.1296T=
ENST00000644527.1:c.*14T= ENSP00000493974.1:n.*14T=
ENST00000644701.1:c.*237T= ENSP00000496097.1:n.*237T=
ENST00000644909.1:c.*519T= ENSP00000493649.1:n.*519T=
ENST00000645152.1:n.1913T=
ENST00000645227.1:c.*938T= ENSP00000495021.1:n.*938T=
ENST00000646242.1:n.7162T=
ENST00000646283.1:c.*14T= ENSP00000494537.1:n.*14T=
ENST00000646401.1:n.2616T=
ENST00000646856.1:c.*1126T= ENSP00000494505.1:n.*1126T=
ENST00000647294.1:c.*1180T= ENSP00000494815.1:n.*1180T=
ENST00000647508.1:c.*14T= ENSP00000496445.1:n.*14T=
ENST00000647515.1:c.*781T= ENSP00000495857.1:n.*781T=
ENST00000348513.10:c.*14T= ENSP00000323967.6:n.*14T=
ENST00000431889.6:c.*14T= ENSP00000445370.1:n.*14T=
ENST00000469334.5:n.1837T=
ENST00000578112.5:c.*1047T= ENSP00000464501.1:n.*1047T=
NM_003079.4:c.*14T= NP_003070.3:n.*14T=
NM_003079.5:c.*14T= MANE Select NP_003070.3:n.*14T=