Canonical Allele Identifier: CA2637750042

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628514-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628514G>C , CM000679.2:g.40628514G>C	GRCh38
NC_000017.10:g.38784766G>C , CM000679.1:g.38784766G>C	GRCh37
NC_000017.9:g.36038292G>C	NCBI36
NG_032163.1:g.24338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1069C>G	ENSP00000466608.2:n.*1069C>G
ENST00000348513.12:c.*271C>G MANE Select	ENSP00000323967.6:n.*271C>G
ENST00000377808.9:c.*494C>G	ENSP00000367039.4:n.*494C>G
ENST00000400122.8:c.*494C>G	ENSP00000411607.2:n.*494C>G
ENST00000469334.6:n.2105C>G
ENST00000578112.6:c.*1304C>G	ENSP00000464501.1:n.*1304C>G
ENST00000580419.6:c.*486C>G	ENSP00000462475.2:n.*486C>G
ENST00000642576.1:n.2650C>G
ENST00000643030.1:n.2130C>G
ENST00000643255.1:c.*3571C>G	ENSP00000493957.1:n.*3571C>G
ENST00000643318.1:c.*271C>G	ENSP00000494771.1:n.*271C>G
ENST00000643378.1:n.2062C>G
ENST00000643683.1:c.*271C>G	ENSP00000496094.1:n.*271C>G
ENST00000643893.1:n.1800C>G
ENST00000644443.1:n.3395C>G
ENST00000644523.1:n.1553C>G
ENST00000644527.1:c.*271C>G	ENSP00000493974.1:n.*271C>G
ENST00000644701.1:c.*494C>G	ENSP00000496097.1:n.*494C>G
ENST00000644909.1:c.*776C>G	ENSP00000493649.1:n.*776C>G
ENST00000645152.1:n.2170C>G
ENST00000645227.1:c.*1195C>G	ENSP00000495021.1:n.*1195C>G
ENST00000646242.1:n.7419C>G
ENST00000646283.1:c.*271C>G	ENSP00000494537.1:n.*271C>G
ENST00000646401.1:n.2873C>G
ENST00000646856.1:c.*1383C>G	ENSP00000494505.1:n.*1383C>G
ENST00000647294.1:c.*1437C>G	ENSP00000494815.1:n.*1437C>G
ENST00000647508.1:c.*271C>G	ENSP00000496445.1:n.*271C>G
ENST00000647515.1:c.*1038C>G	ENSP00000495857.1:n.*1038C>G
ENST00000348513.10:c.*271C>G	ENSP00000323967.6:n.*271C>G
ENST00000431889.6:c.*271C>G	ENSP00000445370.1:n.*271C>G
ENST00000469334.5:n.2094C>G
ENST00000578112.5:c.*1304C>G	ENSP00000464501.1:n.*1304C>G
NM_003079.4:c.*271C>G	NP_003070.3:n.*271C>G
NM_003079.5:c.*271C>G MANE Select	NP_003070.3:n.*271C>G