Canonical Allele Identifier: CA2259640458
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628710C= , CM000679.2:g.40628710C= GRCh38
NC_000017.10:g.38784962C= , CM000679.1:g.38784962C= GRCh37
NC_000017.9:g.36038488C= NCBI36
NG_032163.1:g.24142G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*873G= ENSP00000466608.2:n.*873G=
ENST00000348513.12:c.*75G= MANE Select ENSP00000323967.6:n.*75G=
ENST00000377808.9:c.*298G= ENSP00000367039.4:n.*298G=
ENST00000400122.8:c.*298G= ENSP00000411607.2:n.*298G=
ENST00000469334.6:n.1909G=
ENST00000578112.6:c.*1108G= ENSP00000464501.1:n.*1108G=
ENST00000580419.6:c.*290G= ENSP00000462475.2:n.*290G=
ENST00000642576.1:n.2454G=
ENST00000643030.1:n.1934G=
ENST00000643255.1:c.*3375G= ENSP00000493957.1:n.*3375G=
ENST00000643318.1:c.*75G= ENSP00000494771.1:n.*75G=
ENST00000643378.1:n.1866G=
ENST00000643683.1:c.*75G= ENSP00000496094.1:n.*75G=
ENST00000643893.1:n.1604G=
ENST00000644443.1:n.3199G=
ENST00000644523.1:n.1357G=
ENST00000644527.1:c.*75G= ENSP00000493974.1:n.*75G=
ENST00000644701.1:c.*298G= ENSP00000496097.1:n.*298G=
ENST00000644909.1:c.*580G= ENSP00000493649.1:n.*580G=
ENST00000645152.1:n.1974G=
ENST00000645227.1:c.*999G= ENSP00000495021.1:n.*999G=
ENST00000646242.1:n.7223G=
ENST00000646283.1:c.*75G= ENSP00000494537.1:n.*75G=
ENST00000646401.1:n.2677G=
ENST00000646856.1:c.*1187G= ENSP00000494505.1:n.*1187G=
ENST00000647294.1:c.*1241G= ENSP00000494815.1:n.*1241G=
ENST00000647508.1:c.*75G= ENSP00000496445.1:n.*75G=
ENST00000647515.1:c.*842G= ENSP00000495857.1:n.*842G=
ENST00000348513.10:c.*75G= ENSP00000323967.6:n.*75G=
ENST00000431889.6:c.*75G= ENSP00000445370.1:n.*75G=
ENST00000469334.5:n.1898G=
ENST00000578112.5:c.*1108G= ENSP00000464501.1:n.*1108G=
NM_003079.4:c.*75G= NP_003070.3:n.*75G=
NM_003079.5:c.*75G= MANE Select NP_003070.3:n.*75G=