Canonical Allele Identifier: CA2259640399

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628540A= , CM000679.2:g.40628540A=	GRCh38
NC_000017.10:g.38784792A= , CM000679.1:g.38784792A=	GRCh37
NC_000017.9:g.36038318A=	NCBI36
NG_032163.1:g.24312T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1043T=	ENSP00000466608.2:n.*1043T=
ENST00000348513.12:c.*245T= MANE Select	ENSP00000323967.6:n.*245T=
ENST00000377808.9:c.*468T=	ENSP00000367039.4:n.*468T=
ENST00000400122.8:c.*468T=	ENSP00000411607.2:n.*468T=
ENST00000469334.6:n.2079T=
ENST00000578112.6:c.*1278T=	ENSP00000464501.1:n.*1278T=
ENST00000580419.6:c.*460T=	ENSP00000462475.2:n.*460T=
ENST00000642576.1:n.2624T=
ENST00000643030.1:n.2104T=
ENST00000643255.1:c.*3545T=	ENSP00000493957.1:n.*3545T=
ENST00000643318.1:c.*245T=	ENSP00000494771.1:n.*245T=
ENST00000643378.1:n.2036T=
ENST00000643683.1:c.*245T=	ENSP00000496094.1:n.*245T=
ENST00000643893.1:n.1774T=
ENST00000644443.1:n.3369T=
ENST00000644523.1:n.1527T=
ENST00000644527.1:c.*245T=	ENSP00000493974.1:n.*245T=
ENST00000644701.1:c.*468T=	ENSP00000496097.1:n.*468T=
ENST00000644909.1:c.*750T=	ENSP00000493649.1:n.*750T=
ENST00000645152.1:n.2144T=
ENST00000645227.1:c.*1169T=	ENSP00000495021.1:n.*1169T=
ENST00000646242.1:n.7393T=
ENST00000646283.1:c.*245T=	ENSP00000494537.1:n.*245T=
ENST00000646401.1:n.2847T=
ENST00000646856.1:c.*1357T=	ENSP00000494505.1:n.*1357T=
ENST00000647294.1:c.*1411T=	ENSP00000494815.1:n.*1411T=
ENST00000647508.1:c.*245T=	ENSP00000496445.1:n.*245T=
ENST00000647515.1:c.*1012T=	ENSP00000495857.1:n.*1012T=
ENST00000348513.10:c.*245T=	ENSP00000323967.6:n.*245T=
ENST00000431889.6:c.*245T=	ENSP00000445370.1:n.*245T=
ENST00000469334.5:n.2068T=
ENST00000578112.5:c.*1278T=	ENSP00000464501.1:n.*1278T=
NM_003079.4:c.*245T=	NP_003070.3:n.*245T=
NM_003079.5:c.*245T= MANE Select	NP_003070.3:n.*245T=