Canonical Allele Identifier: CA2576261809

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628688-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628688G>T , CM000679.2:g.40628688G>T	GRCh38
NC_000017.10:g.38784940G>T , CM000679.1:g.38784940G>T	GRCh37
NC_000017.9:g.36038466G>T	NCBI36
NG_032163.1:g.24164C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*895C>A	ENSP00000466608.2:n.*895C>A
ENST00000348513.12:c.*97C>A MANE Select	ENSP00000323967.6:n.*97C>A
ENST00000377808.9:c.*320C>A	ENSP00000367039.4:n.*320C>A
ENST00000400122.8:c.*320C>A	ENSP00000411607.2:n.*320C>A
ENST00000469334.6:n.1931C>A
ENST00000578112.6:c.*1130C>A	ENSP00000464501.1:n.*1130C>A
ENST00000580419.6:c.*312C>A	ENSP00000462475.2:n.*312C>A
ENST00000642576.1:n.2476C>A
ENST00000643030.1:n.1956C>A
ENST00000643255.1:c.*3397C>A	ENSP00000493957.1:n.*3397C>A
ENST00000643318.1:c.*97C>A	ENSP00000494771.1:n.*97C>A
ENST00000643378.1:n.1888C>A
ENST00000643683.1:c.*97C>A	ENSP00000496094.1:n.*97C>A
ENST00000643893.1:n.1626C>A
ENST00000644443.1:n.3221C>A
ENST00000644523.1:n.1379C>A
ENST00000644527.1:c.*97C>A	ENSP00000493974.1:n.*97C>A
ENST00000644701.1:c.*320C>A	ENSP00000496097.1:n.*320C>A
ENST00000644909.1:c.*602C>A	ENSP00000493649.1:n.*602C>A
ENST00000645152.1:n.1996C>A
ENST00000645227.1:c.*1021C>A	ENSP00000495021.1:n.*1021C>A
ENST00000646242.1:n.7245C>A
ENST00000646283.1:c.*97C>A	ENSP00000494537.1:n.*97C>A
ENST00000646401.1:n.2699C>A
ENST00000646856.1:c.*1209C>A	ENSP00000494505.1:n.*1209C>A
ENST00000647294.1:c.*1263C>A	ENSP00000494815.1:n.*1263C>A
ENST00000647508.1:c.*97C>A	ENSP00000496445.1:n.*97C>A
ENST00000647515.1:c.*864C>A	ENSP00000495857.1:n.*864C>A
ENST00000348513.10:c.*97C>A	ENSP00000323967.6:n.*97C>A
ENST00000431889.6:c.*97C>A	ENSP00000445370.1:n.*97C>A
ENST00000469334.5:n.1920C>A
ENST00000578112.5:c.*1130C>A	ENSP00000464501.1:n.*1130C>A
NM_003079.4:c.*97C>A	NP_003070.3:n.*97C>A
NM_003079.5:c.*97C>A MANE Select	NP_003070.3:n.*97C>A