Canonical Allele Identifier: CA2259640523

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628838T= , CM000679.2:g.40628838T=	GRCh38
NC_000017.10:g.38785090T= , CM000679.1:g.38785090T=	GRCh37
NC_000017.9:g.36038616T=	NCBI36
NG_032163.1:g.24014A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*745A=	ENSP00000466608.2:n.*745A=
ENST00000348513.12:c.1183A= MANE Select	ENSP00000323967.6:p.Thr395=
ENST00000377808.9:c.*170A=	ENSP00000367039.4:n.*170A=
ENST00000400122.8:c.*170A=	ENSP00000411607.2:n.*170A=
ENST00000469334.6:n.1781A=
ENST00000578044.6:c.973A=	ENSP00000464511.1:p.Thr325=
ENST00000578112.6:c.*980A=	ENSP00000464501.1:n.*980A=
ENST00000580419.6:c.*162A=	ENSP00000462475.2:n.*162A=
ENST00000642576.1:n.2326A=
ENST00000643030.1:n.1806A=
ENST00000643255.1:c.*3247A=	ENSP00000493957.1:n.*3247A=
ENST00000643318.1:c.973A=	ENSP00000494771.1:p.Thr325=
ENST00000643378.1:n.1738A=
ENST00000643683.1:c.1183A=	ENSP00000496094.1:p.Thr395=
ENST00000643893.1:n.1476A=
ENST00000644443.1:n.3071A=
ENST00000644523.1:n.1229A=
ENST00000644527.1:c.955A=	ENSP00000493974.1:p.Thr319=
ENST00000644701.1:c.*170A=	ENSP00000496097.1:n.*170A=
ENST00000644909.1:c.*452A=	ENSP00000493649.1:n.*452A=
ENST00000645152.1:n.1846A=
ENST00000645227.1:c.*871A=	ENSP00000495021.1:n.*871A=
ENST00000646242.1:n.7095A=
ENST00000646283.1:c.991A=	ENSP00000494537.1:p.Thr331=
ENST00000646401.1:n.2549A=
ENST00000646448.1:n.2457A=
ENST00000646856.1:c.*1059A=	ENSP00000494505.1:n.*1059A=
ENST00000647294.1:c.*1113A=	ENSP00000494815.1:n.*1113A=
ENST00000647508.1:c.1078A=	ENSP00000496445.1:p.Thr360=
ENST00000647515.1:c.*714A=	ENSP00000495857.1:n.*714A=
ENST00000348513.10:c.1183A=	ENSP00000323967.6:p.Thr395=
ENST00000377808.8:c.*170A=	ENSP00000367039.4:n.*170A=
ENST00000400122.7:c.*170A=	ENSP00000411607.2:n.*170A=
ENST00000431889.6:c.1129A=	ENSP00000445370.1:p.Thr377=
ENST00000469334.5:n.1770A=
ENST00000476049.1:c.*1531A=	ENSP00000463483.1:n.*1531A=
ENST00000578044.5:c.973A=	ENSP00000464511.1:p.Thr325=
ENST00000578112.5:c.*980A=	ENSP00000464501.1:n.*980A=
ENST00000580419.5:c.1078A=	ENSP00000462475.1:p.Thr360=
NM_003079.4:c.1183A=	NP_003070.3:p.Thr395=
NM_003079.5:c.1183A= MANE Select	NP_003070.3:p.Thr395=