Canonical Allele Identifier: CA2637750079

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628566-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628566G>A , CM000679.2:g.40628566G>A	GRCh38
NC_000017.10:g.38784818G>A , CM000679.1:g.38784818G>A	GRCh37
NC_000017.9:g.36038344G>A	NCBI36
NG_032163.1:g.24286C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1017C>T	ENSP00000466608.2:n.*1017C>T
ENST00000348513.12:c.*219C>T MANE Select	ENSP00000323967.6:n.*219C>T
ENST00000377808.9:c.*442C>T	ENSP00000367039.4:n.*442C>T
ENST00000400122.8:c.*442C>T	ENSP00000411607.2:n.*442C>T
ENST00000469334.6:n.2053C>T
ENST00000578112.6:c.*1252C>T	ENSP00000464501.1:n.*1252C>T
ENST00000580419.6:c.*434C>T	ENSP00000462475.2:n.*434C>T
ENST00000642576.1:n.2598C>T
ENST00000643030.1:n.2078C>T
ENST00000643255.1:c.*3519C>T	ENSP00000493957.1:n.*3519C>T
ENST00000643318.1:c.*219C>T	ENSP00000494771.1:n.*219C>T
ENST00000643378.1:n.2010C>T
ENST00000643683.1:c.*219C>T	ENSP00000496094.1:n.*219C>T
ENST00000643893.1:n.1748C>T
ENST00000644443.1:n.3343C>T
ENST00000644523.1:n.1501C>T
ENST00000644527.1:c.*219C>T	ENSP00000493974.1:n.*219C>T
ENST00000644701.1:c.*442C>T	ENSP00000496097.1:n.*442C>T
ENST00000644909.1:c.*724C>T	ENSP00000493649.1:n.*724C>T
ENST00000645152.1:n.2118C>T
ENST00000645227.1:c.*1143C>T	ENSP00000495021.1:n.*1143C>T
ENST00000646242.1:n.7367C>T
ENST00000646283.1:c.*219C>T	ENSP00000494537.1:n.*219C>T
ENST00000646401.1:n.2821C>T
ENST00000646856.1:c.*1331C>T	ENSP00000494505.1:n.*1331C>T
ENST00000647294.1:c.*1385C>T	ENSP00000494815.1:n.*1385C>T
ENST00000647508.1:c.*219C>T	ENSP00000496445.1:n.*219C>T
ENST00000647515.1:c.*986C>T	ENSP00000495857.1:n.*986C>T
ENST00000348513.10:c.*219C>T	ENSP00000323967.6:n.*219C>T
ENST00000431889.6:c.*219C>T	ENSP00000445370.1:n.*219C>T
ENST00000469334.5:n.2042C>T
ENST00000578112.5:c.*1252C>T	ENSP00000464501.1:n.*1252C>T
NM_003079.4:c.*219C>T	NP_003070.3:n.*219C>T
NM_003079.5:c.*219C>T MANE Select	NP_003070.3:n.*219C>T