Canonical Allele Identifier: CA2259640398

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628537T= , CM000679.2:g.40628537T=	GRCh38
NC_000017.10:g.38784789T= , CM000679.1:g.38784789T=	GRCh37
NC_000017.9:g.36038315T=	NCBI36
NG_032163.1:g.24315A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1046A=	ENSP00000466608.2:n.*1046A=
ENST00000348513.12:c.*248A= MANE Select	ENSP00000323967.6:n.*248A=
ENST00000377808.9:c.*471A=	ENSP00000367039.4:n.*471A=
ENST00000400122.8:c.*471A=	ENSP00000411607.2:n.*471A=
ENST00000469334.6:n.2082A=
ENST00000578112.6:c.*1281A=	ENSP00000464501.1:n.*1281A=
ENST00000580419.6:c.*463A=	ENSP00000462475.2:n.*463A=
ENST00000642576.1:n.2627A=
ENST00000643030.1:n.2107A=
ENST00000643255.1:c.*3548A=	ENSP00000493957.1:n.*3548A=
ENST00000643318.1:c.*248A=	ENSP00000494771.1:n.*248A=
ENST00000643378.1:n.2039A=
ENST00000643683.1:c.*248A=	ENSP00000496094.1:n.*248A=
ENST00000643893.1:n.1777A=
ENST00000644443.1:n.3372A=
ENST00000644523.1:n.1530A=
ENST00000644527.1:c.*248A=	ENSP00000493974.1:n.*248A=
ENST00000644701.1:c.*471A=	ENSP00000496097.1:n.*471A=
ENST00000644909.1:c.*753A=	ENSP00000493649.1:n.*753A=
ENST00000645152.1:n.2147A=
ENST00000645227.1:c.*1172A=	ENSP00000495021.1:n.*1172A=
ENST00000646242.1:n.7396A=
ENST00000646283.1:c.*248A=	ENSP00000494537.1:n.*248A=
ENST00000646401.1:n.2850A=
ENST00000646856.1:c.*1360A=	ENSP00000494505.1:n.*1360A=
ENST00000647294.1:c.*1414A=	ENSP00000494815.1:n.*1414A=
ENST00000647508.1:c.*248A=	ENSP00000496445.1:n.*248A=
ENST00000647515.1:c.*1015A=	ENSP00000495857.1:n.*1015A=
ENST00000348513.10:c.*248A=	ENSP00000323967.6:n.*248A=
ENST00000431889.6:c.*248A=	ENSP00000445370.1:n.*248A=
ENST00000469334.5:n.2071A=
ENST00000578112.5:c.*1281A=	ENSP00000464501.1:n.*1281A=
NM_003079.4:c.*248A=	NP_003070.3:n.*248A=
NM_003079.5:c.*248A= MANE Select	NP_003070.3:n.*248A=