Canonical Allele Identifier: CA2259640363

Gene: SMARCE1

Linked Data

• dbSNP Id: rs2037056592

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628422T>C , CM000679.2:g.40628422T>C	GRCh38
NC_000017.10:g.38784674T>C , CM000679.1:g.38784674T>C	GRCh37
NC_000017.9:g.36038200T>C	NCBI36
NG_032163.1:g.24430A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1161A>G	ENSP00000466608.2:n.*1161A>G
ENST00000348513.12:c.*363A>G MANE Select	ENSP00000323967.6:n.*363A>G
ENST00000377808.9:c.*586A>G	ENSP00000367039.4:n.*586A>G
ENST00000400122.8:c.*586A>G	ENSP00000411607.2:n.*586A>G
ENST00000469334.6:n.2197A>G
ENST00000578112.6:c.*1396A>G	ENSP00000464501.1:n.*1396A>G
ENST00000580419.6:c.*578A>G	ENSP00000462475.2:n.*578A>G
ENST00000642576.1:n.2742A>G
ENST00000643030.1:n.2222A>G
ENST00000643255.1:c.*3663A>G	ENSP00000493957.1:n.*3663A>G
ENST00000643318.1:c.*363A>G	ENSP00000494771.1:n.*363A>G
ENST00000643378.1:n.2154A>G
ENST00000643683.1:c.*363A>G	ENSP00000496094.1:n.*363A>G
ENST00000643893.1:n.1892A>G
ENST00000644443.1:n.3487A>G
ENST00000644523.1:n.1645A>G
ENST00000644527.1:c.*363A>G	ENSP00000493974.1:n.*363A>G
ENST00000644701.1:c.*586A>G	ENSP00000496097.1:n.*586A>G
ENST00000644909.1:c.*868A>G	ENSP00000493649.1:n.*868A>G
ENST00000645152.1:n.2262A>G
ENST00000645227.1:c.*1287A>G	ENSP00000495021.1:n.*1287A>G
ENST00000646242.1:n.7511A>G
ENST00000646283.1:c.*363A>G	ENSP00000494537.1:n.*363A>G
ENST00000646401.1:n.2965A>G
ENST00000646856.1:c.*1475A>G	ENSP00000494505.1:n.*1475A>G
ENST00000647294.1:c.*1529A>G	ENSP00000494815.1:n.*1529A>G
ENST00000647508.1:c.*363A>G	ENSP00000496445.1:n.*363A>G
ENST00000647515.1:c.*1130A>G	ENSP00000495857.1:n.*1130A>G
ENST00000348513.10:c.*363A>G	ENSP00000323967.6:n.*363A>G
ENST00000578112.5:c.*1396A>G	ENSP00000464501.1:n.*1396A>G
NM_003079.4:c.*363A>G	NP_003070.3:n.*363A>G
NM_003079.5:c.*363A>G MANE Select	NP_003070.3:n.*363A>G