Canonical Allele Identifier: CA2259640368
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628451A= , CM000679.2:g.40628451A= GRCh38
NC_000017.10:g.38784703A= , CM000679.1:g.38784703A= GRCh37
NC_000017.9:g.36038229A= NCBI36
NG_032163.1:g.24401T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*1132T= ENSP00000466608.2:n.*1132T=
ENST00000348513.12:c.*334T= MANE Select ENSP00000323967.6:n.*334T=
ENST00000377808.9:c.*557T= ENSP00000367039.4:n.*557T=
ENST00000400122.8:c.*557T= ENSP00000411607.2:n.*557T=
ENST00000469334.6:n.2168T=
ENST00000578112.6:c.*1367T= ENSP00000464501.1:n.*1367T=
ENST00000580419.6:c.*549T= ENSP00000462475.2:n.*549T=
ENST00000642576.1:n.2713T=
ENST00000643030.1:n.2193T=
ENST00000643255.1:c.*3634T= ENSP00000493957.1:n.*3634T=
ENST00000643318.1:c.*334T= ENSP00000494771.1:n.*334T=
ENST00000643378.1:n.2125T=
ENST00000643683.1:c.*334T= ENSP00000496094.1:n.*334T=
ENST00000643893.1:n.1863T=
ENST00000644443.1:n.3458T=
ENST00000644523.1:n.1616T=
ENST00000644527.1:c.*334T= ENSP00000493974.1:n.*334T=
ENST00000644701.1:c.*557T= ENSP00000496097.1:n.*557T=
ENST00000644909.1:c.*839T= ENSP00000493649.1:n.*839T=
ENST00000645152.1:n.2233T=
ENST00000645227.1:c.*1258T= ENSP00000495021.1:n.*1258T=
ENST00000646242.1:n.7482T=
ENST00000646283.1:c.*334T= ENSP00000494537.1:n.*334T=
ENST00000646401.1:n.2936T=
ENST00000646856.1:c.*1446T= ENSP00000494505.1:n.*1446T=
ENST00000647294.1:c.*1500T= ENSP00000494815.1:n.*1500T=
ENST00000647508.1:c.*334T= ENSP00000496445.1:n.*334T=
ENST00000647515.1:c.*1101T= ENSP00000495857.1:n.*1101T=
ENST00000348513.10:c.*334T= ENSP00000323967.6:n.*334T=
ENST00000578112.5:c.*1367T= ENSP00000464501.1:n.*1367T=
NM_003079.4:c.*334T= NP_003070.3:n.*334T=
NM_003079.5:c.*334T= MANE Select NP_003070.3:n.*334T=