Canonical Allele Identifier: CA2733212343

Gene: SMARCE1

Linked Data

• dbSNP Id: rs772416345

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628769C>T , CM000679.2:g.40628769C>T	GRCh38
NC_000017.10:g.38785021C>T , CM000679.1:g.38785021C>T	GRCh37
NC_000017.9:g.36038547C>T	NCBI36
NG_032163.1:g.24083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*814G>A	ENSP00000466608.2:n.*814G>A
ENST00000348513.12:c.*16G>A MANE Select	ENSP00000323967.6:n.*16G>A
ENST00000377808.9:c.*239G>A	ENSP00000367039.4:n.*239G>A
ENST00000400122.8:c.*239G>A	ENSP00000411607.2:n.*239G>A
ENST00000469334.6:n.1850G>A
ENST00000578112.6:c.*1049G>A	ENSP00000464501.1:n.*1049G>A
ENST00000580419.6:c.*231G>A	ENSP00000462475.2:n.*231G>A
ENST00000642576.1:n.2395G>A
ENST00000643030.1:n.1875G>A
ENST00000643255.1:c.*3316G>A	ENSP00000493957.1:n.*3316G>A
ENST00000643318.1:c.*16G>A	ENSP00000494771.1:n.*16G>A
ENST00000643378.1:n.1807G>A
ENST00000643683.1:c.*16G>A	ENSP00000496094.1:n.*16G>A
ENST00000643893.1:n.1545G>A
ENST00000644443.1:n.3140G>A
ENST00000644523.1:n.1298G>A
ENST00000644527.1:c.*16G>A	ENSP00000493974.1:n.*16G>A
ENST00000644701.1:c.*239G>A	ENSP00000496097.1:n.*239G>A
ENST00000644909.1:c.*521G>A	ENSP00000493649.1:n.*521G>A
ENST00000645152.1:n.1915G>A
ENST00000645227.1:c.*940G>A	ENSP00000495021.1:n.*940G>A
ENST00000646242.1:n.7164G>A
ENST00000646283.1:c.*16G>A	ENSP00000494537.1:n.*16G>A
ENST00000646401.1:n.2618G>A
ENST00000646856.1:c.*1128G>A	ENSP00000494505.1:n.*1128G>A
ENST00000647294.1:c.*1182G>A	ENSP00000494815.1:n.*1182G>A
ENST00000647508.1:c.*16G>A	ENSP00000496445.1:n.*16G>A
ENST00000647515.1:c.*783G>A	ENSP00000495857.1:n.*783G>A
ENST00000348513.10:c.*16G>A	ENSP00000323967.6:n.*16G>A
ENST00000431889.6:c.*16G>A	ENSP00000445370.1:n.*16G>A
ENST00000469334.5:n.1839G>A
ENST00000578112.5:c.*1049G>A	ENSP00000464501.1:n.*1049G>A
NM_003079.4:c.*16G>A	NP_003070.3:n.*16G>A
NM_003079.5:c.*16G>A MANE Select	NP_003070.3:n.*16G>A