Canonical Allele Identifier: CA2259640382

Gene: SMARCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628477A= , CM000679.2:g.40628477A=	GRCh38
NC_000017.10:g.38784729A= , CM000679.1:g.38784729A=	GRCh37
NC_000017.9:g.36038255A=	NCBI36
NG_032163.1:g.24375T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1106T=	ENSP00000466608.2:n.*1106T=
ENST00000348513.12:c.*308T= MANE Select	ENSP00000323967.6:n.*308T=
ENST00000377808.9:c.*531T=	ENSP00000367039.4:n.*531T=
ENST00000400122.8:c.*531T=	ENSP00000411607.2:n.*531T=
ENST00000469334.6:n.2142T=
ENST00000578112.6:c.*1341T=	ENSP00000464501.1:n.*1341T=
ENST00000580419.6:c.*523T=	ENSP00000462475.2:n.*523T=
ENST00000642576.1:n.2687T=
ENST00000643030.1:n.2167T=
ENST00000643255.1:c.*3608T=	ENSP00000493957.1:n.*3608T=
ENST00000643318.1:c.*308T=	ENSP00000494771.1:n.*308T=
ENST00000643378.1:n.2099T=
ENST00000643683.1:c.*308T=	ENSP00000496094.1:n.*308T=
ENST00000643893.1:n.1837T=
ENST00000644443.1:n.3432T=
ENST00000644523.1:n.1590T=
ENST00000644527.1:c.*308T=	ENSP00000493974.1:n.*308T=
ENST00000644701.1:c.*531T=	ENSP00000496097.1:n.*531T=
ENST00000644909.1:c.*813T=	ENSP00000493649.1:n.*813T=
ENST00000645152.1:n.2207T=
ENST00000645227.1:c.*1232T=	ENSP00000495021.1:n.*1232T=
ENST00000646242.1:n.7456T=
ENST00000646283.1:c.*308T=	ENSP00000494537.1:n.*308T=
ENST00000646401.1:n.2910T=
ENST00000646856.1:c.*1420T=	ENSP00000494505.1:n.*1420T=
ENST00000647294.1:c.*1474T=	ENSP00000494815.1:n.*1474T=
ENST00000647508.1:c.*308T=	ENSP00000496445.1:n.*308T=
ENST00000647515.1:c.*1075T=	ENSP00000495857.1:n.*1075T=
ENST00000348513.10:c.*308T=	ENSP00000323967.6:n.*308T=
ENST00000431889.6:c.*308T=	ENSP00000445370.1:n.*308T=
ENST00000578112.5:c.*1341T=	ENSP00000464501.1:n.*1341T=
NM_003079.4:c.*308T=	NP_003070.3:n.*308T=
NM_003079.5:c.*308T= MANE Select	NP_003070.3:n.*308T=