Canonical Allele Identifier: CA2637750082

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628568-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628568C>A , CM000679.2:g.40628568C>A	GRCh38
NC_000017.10:g.38784820C>A , CM000679.1:g.38784820C>A	GRCh37
NC_000017.9:g.36038346C>A	NCBI36
NG_032163.1:g.24284G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1015G>T	ENSP00000466608.2:n.*1015G>T
ENST00000348513.12:c.*217G>T MANE Select	ENSP00000323967.6:n.*217G>T
ENST00000377808.9:c.*440G>T	ENSP00000367039.4:n.*440G>T
ENST00000400122.8:c.*440G>T	ENSP00000411607.2:n.*440G>T
ENST00000469334.6:n.2051G>T
ENST00000578112.6:c.*1250G>T	ENSP00000464501.1:n.*1250G>T
ENST00000580419.6:c.*432G>T	ENSP00000462475.2:n.*432G>T
ENST00000642576.1:n.2596G>T
ENST00000643030.1:n.2076G>T
ENST00000643255.1:c.*3517G>T	ENSP00000493957.1:n.*3517G>T
ENST00000643318.1:c.*217G>T	ENSP00000494771.1:n.*217G>T
ENST00000643378.1:n.2008G>T
ENST00000643683.1:c.*217G>T	ENSP00000496094.1:n.*217G>T
ENST00000643893.1:n.1746G>T
ENST00000644443.1:n.3341G>T
ENST00000644523.1:n.1499G>T
ENST00000644527.1:c.*217G>T	ENSP00000493974.1:n.*217G>T
ENST00000644701.1:c.*440G>T	ENSP00000496097.1:n.*440G>T
ENST00000644909.1:c.*722G>T	ENSP00000493649.1:n.*722G>T
ENST00000645152.1:n.2116G>T
ENST00000645227.1:c.*1141G>T	ENSP00000495021.1:n.*1141G>T
ENST00000646242.1:n.7365G>T
ENST00000646283.1:c.*217G>T	ENSP00000494537.1:n.*217G>T
ENST00000646401.1:n.2819G>T
ENST00000646856.1:c.*1329G>T	ENSP00000494505.1:n.*1329G>T
ENST00000647294.1:c.*1383G>T	ENSP00000494815.1:n.*1383G>T
ENST00000647508.1:c.*217G>T	ENSP00000496445.1:n.*217G>T
ENST00000647515.1:c.*984G>T	ENSP00000495857.1:n.*984G>T
ENST00000348513.10:c.*217G>T	ENSP00000323967.6:n.*217G>T
ENST00000431889.6:c.*217G>T	ENSP00000445370.1:n.*217G>T
ENST00000469334.5:n.2040G>T
ENST00000578112.5:c.*1250G>T	ENSP00000464501.1:n.*1250G>T
NM_003079.4:c.*217G>T	NP_003070.3:n.*217G>T
NM_003079.5:c.*217G>T MANE Select	NP_003070.3:n.*217G>T