Canonical Allele Identifier: CA2259640356
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628410G= , CM000679.2:g.40628410G= GRCh38
NC_000017.10:g.38784662G= , CM000679.1:g.38784662G= GRCh37
NC_000017.9:g.36038188G= NCBI36
NG_032163.1:g.24442C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*1173C= ENSP00000466608.2:n.*1173C=
ENST00000348513.12:c.*375C= MANE Select ENSP00000323967.6:n.*375C=
ENST00000377808.9:c.*598C= ENSP00000367039.4:n.*598C=
ENST00000400122.8:c.*598C= ENSP00000411607.2:n.*598C=
ENST00000469334.6:n.2209C=
ENST00000578112.6:c.*1408C= ENSP00000464501.1:n.*1408C=
ENST00000580419.6:c.*590C= ENSP00000462475.2:n.*590C=
ENST00000642576.1:n.2754C=
ENST00000643030.1:n.2234C=
ENST00000643255.1:c.*3675C= ENSP00000493957.1:n.*3675C=
ENST00000643318.1:c.*375C= ENSP00000494771.1:n.*375C=
ENST00000643378.1:n.2166C=
ENST00000643683.1:c.*375C= ENSP00000496094.1:n.*375C=
ENST00000643893.1:n.1904C=
ENST00000644443.1:n.3499C=
ENST00000644523.1:n.1657C=
ENST00000644527.1:c.*375C= ENSP00000493974.1:n.*375C=
ENST00000644701.1:c.*598C= ENSP00000496097.1:n.*598C=
ENST00000644909.1:c.*880C= ENSP00000493649.1:n.*880C=
ENST00000645152.1:n.2274C=
ENST00000645227.1:c.*1299C= ENSP00000495021.1:n.*1299C=
ENST00000646242.1:n.7523C=
ENST00000646283.1:c.*375C= ENSP00000494537.1:n.*375C=
ENST00000646401.1:n.2977C=
ENST00000646856.1:c.*1487C= ENSP00000494505.1:n.*1487C=
ENST00000647294.1:c.*1541C= ENSP00000494815.1:n.*1541C=
ENST00000647508.1:c.*375C= ENSP00000496445.1:n.*375C=
ENST00000647515.1:c.*1142C= ENSP00000495857.1:n.*1142C=
ENST00000348513.10:c.*375C= ENSP00000323967.6:n.*375C=
ENST00000578112.5:c.*1408C= ENSP00000464501.1:n.*1408C=
NM_003079.4:c.*375C= NP_003070.3:n.*375C=
NM_003079.5:c.*375C= MANE Select NP_003070.3:n.*375C=