Canonical Allele Identifier: CA2259640349

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628383A= , CM000679.2:g.40628383A=	GRCh38
NC_000017.10:g.38784635A= , CM000679.1:g.38784635A=	GRCh37
NC_000017.9:g.36038161A=	NCBI36
NG_032163.1:g.24469T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1200T=	ENSP00000466608.2:n.*1200T=
ENST00000348513.12:c.*402T= MANE Select	ENSP00000323967.6:n.*402T=
ENST00000377808.9:c.*625T=	ENSP00000367039.4:n.*625T=
ENST00000400122.8:c.*625T=	ENSP00000411607.2:n.*625T=
ENST00000469334.6:n.2236T=
ENST00000578112.6:c.*1435T=	ENSP00000464501.1:n.*1435T=
ENST00000580419.6:c.*617T=	ENSP00000462475.2:n.*617T=
ENST00000642576.1:n.2781T=
ENST00000643030.1:n.2261T=
ENST00000643255.1:c.*3702T=	ENSP00000493957.1:n.*3702T=
ENST00000643318.1:c.*402T=	ENSP00000494771.1:n.*402T=
ENST00000643378.1:n.2193T=
ENST00000643683.1:c.*402T=	ENSP00000496094.1:n.*402T=
ENST00000643893.1:n.1931T=
ENST00000644443.1:n.3526T=
ENST00000644523.1:n.1684T=
ENST00000644527.1:c.*402T=	ENSP00000493974.1:n.*402T=
ENST00000644701.1:c.*625T=	ENSP00000496097.1:n.*625T=
ENST00000644909.1:c.*907T=	ENSP00000493649.1:n.*907T=
ENST00000645152.1:n.2301T=
ENST00000645227.1:c.*1326T=	ENSP00000495021.1:n.*1326T=
ENST00000646242.1:n.7550T=
ENST00000646283.1:c.*402T=	ENSP00000494537.1:n.*402T=
ENST00000646401.1:n.3004T=
ENST00000646856.1:c.*1514T=	ENSP00000494505.1:n.*1514T=
ENST00000647294.1:c.*1568T=	ENSP00000494815.1:n.*1568T=
ENST00000647508.1:c.*402T=	ENSP00000496445.1:n.*402T=
ENST00000647515.1:c.*1169T=	ENSP00000495857.1:n.*1169T=
ENST00000348513.10:c.*402T=	ENSP00000323967.6:n.*402T=
ENST00000578112.5:c.*1435T=	ENSP00000464501.1:n.*1435T=
NM_003079.4:c.*402T=	NP_003070.3:n.*402T=
NM_003079.5:c.*402T= MANE Select	NP_003070.3:n.*402T=