Canonical Allele Identifier: CA2637750029

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628488-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628488C>T , CM000679.2:g.40628488C>T	GRCh38
NC_000017.10:g.38784740C>T , CM000679.1:g.38784740C>T	GRCh37
NC_000017.9:g.36038266C>T	NCBI36
NG_032163.1:g.24364G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1095G>A	ENSP00000466608.2:n.*1095G>A
ENST00000348513.12:c.*297G>A MANE Select	ENSP00000323967.6:n.*297G>A
ENST00000377808.9:c.*520G>A	ENSP00000367039.4:n.*520G>A
ENST00000400122.8:c.*520G>A	ENSP00000411607.2:n.*520G>A
ENST00000469334.6:n.2131G>A
ENST00000578112.6:c.*1330G>A	ENSP00000464501.1:n.*1330G>A
ENST00000580419.6:c.*512G>A	ENSP00000462475.2:n.*512G>A
ENST00000642576.1:n.2676G>A
ENST00000643030.1:n.2156G>A
ENST00000643255.1:c.*3597G>A	ENSP00000493957.1:n.*3597G>A
ENST00000643318.1:c.*297G>A	ENSP00000494771.1:n.*297G>A
ENST00000643378.1:n.2088G>A
ENST00000643683.1:c.*297G>A	ENSP00000496094.1:n.*297G>A
ENST00000643893.1:n.1826G>A
ENST00000644443.1:n.3421G>A
ENST00000644523.1:n.1579G>A
ENST00000644527.1:c.*297G>A	ENSP00000493974.1:n.*297G>A
ENST00000644701.1:c.*520G>A	ENSP00000496097.1:n.*520G>A
ENST00000644909.1:c.*802G>A	ENSP00000493649.1:n.*802G>A
ENST00000645152.1:n.2196G>A
ENST00000645227.1:c.*1221G>A	ENSP00000495021.1:n.*1221G>A
ENST00000646242.1:n.7445G>A
ENST00000646283.1:c.*297G>A	ENSP00000494537.1:n.*297G>A
ENST00000646401.1:n.2899G>A
ENST00000646856.1:c.*1409G>A	ENSP00000494505.1:n.*1409G>A
ENST00000647294.1:c.*1463G>A	ENSP00000494815.1:n.*1463G>A
ENST00000647508.1:c.*297G>A	ENSP00000496445.1:n.*297G>A
ENST00000647515.1:c.*1064G>A	ENSP00000495857.1:n.*1064G>A
ENST00000348513.10:c.*297G>A	ENSP00000323967.6:n.*297G>A
ENST00000431889.6:c.*297G>A	ENSP00000445370.1:n.*297G>A
ENST00000469334.5:n.2120G>A
ENST00000578112.5:c.*1330G>A	ENSP00000464501.1:n.*1330G>A
NM_003079.4:c.*297G>A	NP_003070.3:n.*297G>A
NM_003079.5:c.*297G>A MANE Select	NP_003070.3:n.*297G>A