Canonical Allele Identifier: CA2637750087

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628577-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628577A>C , CM000679.2:g.40628577A>C	GRCh38
NC_000017.10:g.38784829A>C , CM000679.1:g.38784829A>C	GRCh37
NC_000017.9:g.36038355A>C	NCBI36
NG_032163.1:g.24275T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1006T>G	ENSP00000466608.2:n.*1006T>G
ENST00000348513.12:c.*208T>G MANE Select	ENSP00000323967.6:n.*208T>G
ENST00000377808.9:c.*431T>G	ENSP00000367039.4:n.*431T>G
ENST00000400122.8:c.*431T>G	ENSP00000411607.2:n.*431T>G
ENST00000469334.6:n.2042T>G
ENST00000578112.6:c.*1241T>G	ENSP00000464501.1:n.*1241T>G
ENST00000580419.6:c.*423T>G	ENSP00000462475.2:n.*423T>G
ENST00000642576.1:n.2587T>G
ENST00000643030.1:n.2067T>G
ENST00000643255.1:c.*3508T>G	ENSP00000493957.1:n.*3508T>G
ENST00000643318.1:c.*208T>G	ENSP00000494771.1:n.*208T>G
ENST00000643378.1:n.1999T>G
ENST00000643683.1:c.*208T>G	ENSP00000496094.1:n.*208T>G
ENST00000643893.1:n.1737T>G
ENST00000644443.1:n.3332T>G
ENST00000644523.1:n.1490T>G
ENST00000644527.1:c.*208T>G	ENSP00000493974.1:n.*208T>G
ENST00000644701.1:c.*431T>G	ENSP00000496097.1:n.*431T>G
ENST00000644909.1:c.*713T>G	ENSP00000493649.1:n.*713T>G
ENST00000645152.1:n.2107T>G
ENST00000645227.1:c.*1132T>G	ENSP00000495021.1:n.*1132T>G
ENST00000646242.1:n.7356T>G
ENST00000646283.1:c.*208T>G	ENSP00000494537.1:n.*208T>G
ENST00000646401.1:n.2810T>G
ENST00000646856.1:c.*1320T>G	ENSP00000494505.1:n.*1320T>G
ENST00000647294.1:c.*1374T>G	ENSP00000494815.1:n.*1374T>G
ENST00000647508.1:c.*208T>G	ENSP00000496445.1:n.*208T>G
ENST00000647515.1:c.*975T>G	ENSP00000495857.1:n.*975T>G
ENST00000348513.10:c.*208T>G	ENSP00000323967.6:n.*208T>G
ENST00000431889.6:c.*208T>G	ENSP00000445370.1:n.*208T>G
ENST00000469334.5:n.2031T>G
ENST00000578112.5:c.*1241T>G	ENSP00000464501.1:n.*1241T>G
NM_003079.4:c.*208T>G	NP_003070.3:n.*208T>G
NM_003079.5:c.*208T>G MANE Select	NP_003070.3:n.*208T>G