Canonical Allele Identifier: CA2259640494
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628777G= , CM000679.2:g.40628777G= GRCh38
NC_000017.10:g.38785029G= , CM000679.1:g.38785029G= GRCh37
NC_000017.9:g.36038555G= NCBI36
NG_032163.1:g.24075C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264640.9:c.*806C= ENSP00000466608.2:n.*806C=
ENST00000348513.12:c.*8C= MANE Select ENSP00000323967.6:n.*8C=
ENST00000377808.9:c.*231C= ENSP00000367039.4:n.*231C=
ENST00000400122.8:c.*231C= ENSP00000411607.2:n.*231C=
ENST00000469334.6:n.1842C=
ENST00000578112.6:c.*1041C= ENSP00000464501.1:n.*1041C=
ENST00000580419.6:c.*223C= ENSP00000462475.2:n.*223C=
ENST00000642576.1:n.2387C=
ENST00000643030.1:n.1867C=
ENST00000643255.1:c.*3308C= ENSP00000493957.1:n.*3308C=
ENST00000643318.1:c.*8C= ENSP00000494771.1:n.*8C=
ENST00000643378.1:n.1799C=
ENST00000643683.1:c.*8C= ENSP00000496094.1:n.*8C=
ENST00000643893.1:n.1537C=
ENST00000644443.1:n.3132C=
ENST00000644523.1:n.1290C=
ENST00000644527.1:c.*8C= ENSP00000493974.1:n.*8C=
ENST00000644701.1:c.*231C= ENSP00000496097.1:n.*231C=
ENST00000644909.1:c.*513C= ENSP00000493649.1:n.*513C=
ENST00000645152.1:n.1907C=
ENST00000645227.1:c.*932C= ENSP00000495021.1:n.*932C=
ENST00000646242.1:n.7156C=
ENST00000646283.1:c.*8C= ENSP00000494537.1:n.*8C=
ENST00000646401.1:n.2610C=
ENST00000646448.1:n.2518C=
ENST00000646856.1:c.*1120C= ENSP00000494505.1:n.*1120C=
ENST00000647294.1:c.*1174C= ENSP00000494815.1:n.*1174C=
ENST00000647508.1:c.*8C= ENSP00000496445.1:n.*8C=
ENST00000647515.1:c.*775C= ENSP00000495857.1:n.*775C=
ENST00000348513.10:c.*8C= ENSP00000323967.6:n.*8C=
ENST00000431889.6:c.*8C= ENSP00000445370.1:n.*8C=
ENST00000469334.5:n.1831C=
ENST00000578112.5:c.*1041C= ENSP00000464501.1:n.*1041C=
NM_003079.4:c.*8C= NP_003070.3:n.*8C=
NM_003079.5:c.*8C= MANE Select NP_003070.3:n.*8C=