Canonical Allele Identifier: CA2259640537
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628857G= , CM000679.2:g.40628857G= GRCh38
NC_000017.10:g.38785109G= , CM000679.1:g.38785109G= GRCh37
NC_000017.9:g.36038635G= NCBI36
NG_032163.1:g.23995C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264640.9:c.*726C= ENSP00000466608.2:n.*726C=
ENST00000348513.12:c.1164C= MANE Select ENSP00000323967.6:p.Gly388=
ENST00000377808.9:c.*151C= ENSP00000367039.4:n.*151C=
ENST00000400122.8:c.*151C= ENSP00000411607.2:n.*151C=
ENST00000469334.6:n.1762C=
ENST00000578044.6:c.954C= ENSP00000464511.1:p.Gly318=
ENST00000578112.6:c.*961C= ENSP00000464501.1:n.*961C=
ENST00000580419.6:c.*143C= ENSP00000462475.2:n.*143C=
ENST00000642576.1:n.2307C=
ENST00000643030.1:n.1787C=
ENST00000643255.1:c.*3228C= ENSP00000493957.1:n.*3228C=
ENST00000643318.1:c.954C= ENSP00000494771.1:p.Gly318=
ENST00000643378.1:n.1719C=
ENST00000643683.1:c.1164C= ENSP00000496094.1:p.Gly388=
ENST00000643893.1:n.1457C=
ENST00000644443.1:n.3052C=
ENST00000644523.1:n.1210C=
ENST00000644527.1:c.936C= ENSP00000493974.1:p.Gly312=
ENST00000644701.1:c.*151C= ENSP00000496097.1:n.*151C=
ENST00000644909.1:c.*433C= ENSP00000493649.1:n.*433C=
ENST00000645152.1:n.1827C=
ENST00000645227.1:c.*852C= ENSP00000495021.1:n.*852C=
ENST00000646242.1:n.7076C=
ENST00000646283.1:c.972C= ENSP00000494537.1:p.Gly324=
ENST00000646401.1:n.2530C=
ENST00000646448.1:n.2438C=
ENST00000646856.1:c.*1040C= ENSP00000494505.1:n.*1040C=
ENST00000647294.1:c.*1094C= ENSP00000494815.1:n.*1094C=
ENST00000647508.1:c.1059C= ENSP00000496445.1:p.Gly353=
ENST00000647515.1:c.*695C= ENSP00000495857.1:n.*695C=
ENST00000348513.10:c.1164C= ENSP00000323967.6:p.Gly388=
ENST00000377808.8:c.*151C= ENSP00000367039.4:n.*151C=
ENST00000400122.7:c.*151C= ENSP00000411607.2:n.*151C=
ENST00000431889.6:c.1110C= ENSP00000445370.1:p.Gly370=
ENST00000469334.5:n.1751C=
ENST00000476049.1:c.*1512C= ENSP00000463483.1:n.*1512C=
ENST00000578044.5:c.954C= ENSP00000464511.1:p.Gly318=
ENST00000578112.5:c.*961C= ENSP00000464501.1:n.*961C=
ENST00000580419.5:c.1059C= ENSP00000462475.1:p.Gly353=
NM_003079.4:c.1164C= NP_003070.3:p.Gly388=
NM_003079.5:c.1164C= MANE Select NP_003070.3:p.Gly388=