Canonical Allele Identifier: CA2637750204

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628714-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628714T>G , CM000679.2:g.40628714T>G	GRCh38
NC_000017.10:g.38784966T>G , CM000679.1:g.38784966T>G	GRCh37
NC_000017.9:g.36038492T>G	NCBI36
NG_032163.1:g.24138A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*869A>C	ENSP00000466608.2:n.*869A>C
ENST00000348513.12:c.*71A>C MANE Select	ENSP00000323967.6:n.*71A>C
ENST00000377808.9:c.*294A>C	ENSP00000367039.4:n.*294A>C
ENST00000400122.8:c.*294A>C	ENSP00000411607.2:n.*294A>C
ENST00000469334.6:n.1905A>C
ENST00000578112.6:c.*1104A>C	ENSP00000464501.1:n.*1104A>C
ENST00000580419.6:c.*286A>C	ENSP00000462475.2:n.*286A>C
ENST00000642576.1:n.2450A>C
ENST00000643030.1:n.1930A>C
ENST00000643255.1:c.*3371A>C	ENSP00000493957.1:n.*3371A>C
ENST00000643318.1:c.*71A>C	ENSP00000494771.1:n.*71A>C
ENST00000643378.1:n.1862A>C
ENST00000643683.1:c.*71A>C	ENSP00000496094.1:n.*71A>C
ENST00000643893.1:n.1600A>C
ENST00000644443.1:n.3195A>C
ENST00000644523.1:n.1353A>C
ENST00000644527.1:c.*71A>C	ENSP00000493974.1:n.*71A>C
ENST00000644701.1:c.*294A>C	ENSP00000496097.1:n.*294A>C
ENST00000644909.1:c.*576A>C	ENSP00000493649.1:n.*576A>C
ENST00000645152.1:n.1970A>C
ENST00000645227.1:c.*995A>C	ENSP00000495021.1:n.*995A>C
ENST00000646242.1:n.7219A>C
ENST00000646283.1:c.*71A>C	ENSP00000494537.1:n.*71A>C
ENST00000646401.1:n.2673A>C
ENST00000646856.1:c.*1183A>C	ENSP00000494505.1:n.*1183A>C
ENST00000647294.1:c.*1237A>C	ENSP00000494815.1:n.*1237A>C
ENST00000647508.1:c.*71A>C	ENSP00000496445.1:n.*71A>C
ENST00000647515.1:c.*838A>C	ENSP00000495857.1:n.*838A>C
ENST00000348513.10:c.*71A>C	ENSP00000323967.6:n.*71A>C
ENST00000431889.6:c.*71A>C	ENSP00000445370.1:n.*71A>C
ENST00000469334.5:n.1894A>C
ENST00000578112.5:c.*1104A>C	ENSP00000464501.1:n.*1104A>C
NM_003079.4:c.*71A>C	NP_003070.3:n.*71A>C
NM_003079.5:c.*71A>C MANE Select	NP_003070.3:n.*71A>C