Canonical Allele Identifier: CA2576261813

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628717-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628717C>T , CM000679.2:g.40628717C>T	GRCh38
NC_000017.10:g.38784969C>T , CM000679.1:g.38784969C>T	GRCh37
NC_000017.9:g.36038495C>T	NCBI36
NG_032163.1:g.24135G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*866G>A	ENSP00000466608.2:n.*866G>A
ENST00000348513.12:c.*68G>A MANE Select	ENSP00000323967.6:n.*68G>A
ENST00000377808.9:c.*291G>A	ENSP00000367039.4:n.*291G>A
ENST00000400122.8:c.*291G>A	ENSP00000411607.2:n.*291G>A
ENST00000469334.6:n.1902G>A
ENST00000578112.6:c.*1101G>A	ENSP00000464501.1:n.*1101G>A
ENST00000580419.6:c.*283G>A	ENSP00000462475.2:n.*283G>A
ENST00000642576.1:n.2447G>A
ENST00000643030.1:n.1927G>A
ENST00000643255.1:c.*3368G>A	ENSP00000493957.1:n.*3368G>A
ENST00000643318.1:c.*68G>A	ENSP00000494771.1:n.*68G>A
ENST00000643378.1:n.1859G>A
ENST00000643683.1:c.*68G>A	ENSP00000496094.1:n.*68G>A
ENST00000643893.1:n.1597G>A
ENST00000644443.1:n.3192G>A
ENST00000644523.1:n.1350G>A
ENST00000644527.1:c.*68G>A	ENSP00000493974.1:n.*68G>A
ENST00000644701.1:c.*291G>A	ENSP00000496097.1:n.*291G>A
ENST00000644909.1:c.*573G>A	ENSP00000493649.1:n.*573G>A
ENST00000645152.1:n.1967G>A
ENST00000645227.1:c.*992G>A	ENSP00000495021.1:n.*992G>A
ENST00000646242.1:n.7216G>A
ENST00000646283.1:c.*68G>A	ENSP00000494537.1:n.*68G>A
ENST00000646401.1:n.2670G>A
ENST00000646856.1:c.*1180G>A	ENSP00000494505.1:n.*1180G>A
ENST00000647294.1:c.*1234G>A	ENSP00000494815.1:n.*1234G>A
ENST00000647508.1:c.*68G>A	ENSP00000496445.1:n.*68G>A
ENST00000647515.1:c.*835G>A	ENSP00000495857.1:n.*835G>A
ENST00000348513.10:c.*68G>A	ENSP00000323967.6:n.*68G>A
ENST00000431889.6:c.*68G>A	ENSP00000445370.1:n.*68G>A
ENST00000469334.5:n.1891G>A
ENST00000578112.5:c.*1101G>A	ENSP00000464501.1:n.*1101G>A
NM_003079.4:c.*68G>A	NP_003070.3:n.*68G>A
NM_003079.5:c.*68G>A MANE Select	NP_003070.3:n.*68G>A