Canonical Allele Identifier: CA2637749984

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628413-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628413C>A , CM000679.2:g.40628413C>A	GRCh38
NC_000017.10:g.38784665C>A , CM000679.1:g.38784665C>A	GRCh37
NC_000017.9:g.36038191C>A	NCBI36
NG_032163.1:g.24439G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1170G>T	ENSP00000466608.2:n.*1170G>T
ENST00000348513.12:c.*372G>T MANE Select	ENSP00000323967.6:n.*372G>T
ENST00000377808.9:c.*595G>T	ENSP00000367039.4:n.*595G>T
ENST00000400122.8:c.*595G>T	ENSP00000411607.2:n.*595G>T
ENST00000469334.6:n.2206G>T
ENST00000578112.6:c.*1405G>T	ENSP00000464501.1:n.*1405G>T
ENST00000580419.6:c.*587G>T	ENSP00000462475.2:n.*587G>T
ENST00000642576.1:n.2751G>T
ENST00000643030.1:n.2231G>T
ENST00000643255.1:c.*3672G>T	ENSP00000493957.1:n.*3672G>T
ENST00000643318.1:c.*372G>T	ENSP00000494771.1:n.*372G>T
ENST00000643378.1:n.2163G>T
ENST00000643683.1:c.*372G>T	ENSP00000496094.1:n.*372G>T
ENST00000643893.1:n.1901G>T
ENST00000644443.1:n.3496G>T
ENST00000644523.1:n.1654G>T
ENST00000644527.1:c.*372G>T	ENSP00000493974.1:n.*372G>T
ENST00000644701.1:c.*595G>T	ENSP00000496097.1:n.*595G>T
ENST00000644909.1:c.*877G>T	ENSP00000493649.1:n.*877G>T
ENST00000645152.1:n.2271G>T
ENST00000645227.1:c.*1296G>T	ENSP00000495021.1:n.*1296G>T
ENST00000646242.1:n.7520G>T
ENST00000646283.1:c.*372G>T	ENSP00000494537.1:n.*372G>T
ENST00000646401.1:n.2974G>T
ENST00000646856.1:c.*1484G>T	ENSP00000494505.1:n.*1484G>T
ENST00000647294.1:c.*1538G>T	ENSP00000494815.1:n.*1538G>T
ENST00000647508.1:c.*372G>T	ENSP00000496445.1:n.*372G>T
ENST00000647515.1:c.*1139G>T	ENSP00000495857.1:n.*1139G>T
ENST00000348513.10:c.*372G>T	ENSP00000323967.6:n.*372G>T
ENST00000578112.5:c.*1405G>T	ENSP00000464501.1:n.*1405G>T
NM_003079.4:c.*372G>T	NP_003070.3:n.*372G>T
NM_003079.5:c.*372G>T MANE Select	NP_003070.3:n.*372G>T