Canonical Allele Identifier: CA2259640473

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628735A= , CM000679.2:g.40628735A=	GRCh38
NC_000017.10:g.38784987A= , CM000679.1:g.38784987A=	GRCh37
NC_000017.9:g.36038513A=	NCBI36
NG_032163.1:g.24117T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*848T=	ENSP00000466608.2:n.*848T=
ENST00000348513.12:c.*50T= MANE Select	ENSP00000323967.6:n.*50T=
ENST00000377808.9:c.*273T=	ENSP00000367039.4:n.*273T=
ENST00000400122.8:c.*273T=	ENSP00000411607.2:n.*273T=
ENST00000469334.6:n.1884T=
ENST00000578112.6:c.*1083T=	ENSP00000464501.1:n.*1083T=
ENST00000580419.6:c.*265T=	ENSP00000462475.2:n.*265T=
ENST00000642576.1:n.2429T=
ENST00000643030.1:n.1909T=
ENST00000643255.1:c.*3350T=	ENSP00000493957.1:n.*3350T=
ENST00000643318.1:c.*50T=	ENSP00000494771.1:n.*50T=
ENST00000643378.1:n.1841T=
ENST00000643683.1:c.*50T=	ENSP00000496094.1:n.*50T=
ENST00000643893.1:n.1579T=
ENST00000644443.1:n.3174T=
ENST00000644523.1:n.1332T=
ENST00000644527.1:c.*50T=	ENSP00000493974.1:n.*50T=
ENST00000644701.1:c.*273T=	ENSP00000496097.1:n.*273T=
ENST00000644909.1:c.*555T=	ENSP00000493649.1:n.*555T=
ENST00000645152.1:n.1949T=
ENST00000645227.1:c.*974T=	ENSP00000495021.1:n.*974T=
ENST00000646242.1:n.7198T=
ENST00000646283.1:c.*50T=	ENSP00000494537.1:n.*50T=
ENST00000646401.1:n.2652T=
ENST00000646856.1:c.*1162T=	ENSP00000494505.1:n.*1162T=
ENST00000647294.1:c.*1216T=	ENSP00000494815.1:n.*1216T=
ENST00000647508.1:c.*50T=	ENSP00000496445.1:n.*50T=
ENST00000647515.1:c.*817T=	ENSP00000495857.1:n.*817T=
ENST00000348513.10:c.*50T=	ENSP00000323967.6:n.*50T=
ENST00000431889.6:c.*50T=	ENSP00000445370.1:n.*50T=
ENST00000469334.5:n.1873T=
ENST00000578112.5:c.*1083T=	ENSP00000464501.1:n.*1083T=
NM_003079.4:c.*50T=	NP_003070.3:n.*50T=
NM_003079.5:c.*50T= MANE Select	NP_003070.3:n.*50T=